Immuno hard to recall Flashcards

1
Q

What type of anaphylaxis does aspirin cause? What is another name for this?

A

Non-IgE mediated anaphylaxis

Mast cell degranulation

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2
Q

Difference between acute vs chronic urticaria?

A
Acute = <6 weeks intermittent rash which appears in same site for <24 hours each time
Chronic = >6 weeks
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3
Q

When would an urticarial rash make you suspicious of an underlying vasculitis?

A

If it lasts more than 24 hours in a single site

If it resolves with bruising or skin depigmentation

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4
Q

What does C1 inhibitor deficiency cause?

A

acquired angioedema

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5
Q

What dose of adrenaline should be given in anaphylaxis?

A

IM 1ml of 1:1000 (i.e. 1mg/ml)

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6
Q

Kostmanns syndrome is a congenital deficiency of which component of the immune system?

A

Neutrophil

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7
Q

Which infection is most common as a consequence of B cell deficiency?

A

Bacterial

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8
Q

Meningococcal infections are quite common as a result of which deficiency of the component of the immune system?

A

Complement

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9
Q

A complete deficiency in this molecule is associated with recurrent respiratory and gastrointestinal infections

A

IgA

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10
Q

Leukocyte Adhesion Deficiency is characterised by a very high count in which cell line?

A

neutrophils

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11
Q

Which crucial enzyme is vital for the oxidative killing of intracellular micro-organisms?

A

NADPH oxidase

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12
Q

Which complement factor is an important chemotaxic agent?

A

C3a

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13
Q

What type of hypersensitivity reaction is RA?

A

Type IV – T-cell mediated

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14
Q

What type of hypersensitivity reaction is T1DM?

A

Type IV – T-cell mediated

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15
Q

What type of hypersensitivity reaction is ITP?

A

Type II – Antibody mediated

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16
Q

What type of hypersensitivity reaction is Hepatitis C associated membranoproliferative glomerulonephritis type I?

A

Type III – Immune complex mediated

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17
Q

What type of hypersensitivity reaction is Goodpasture’s?

A

Type II – Antibody mediated

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18
Q

What type of hypersensitivity reaction is MG?

A

Type II – Antibody mediated

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19
Q

Antibody in SLE?

A

Anti-dsDNA

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20
Q

Antibody in Wegener’s?

A

c-ANCA

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21
Q

Antibody in RA?

A

anti-CCP

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22
Q

Antibody in PBC?

A

AMA

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23
Q

What is the specific auto-antigen that is the target of the immune system in goodpasture’s?

A

Type IV collagen

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24
Q

Tx for goodpasture’s?

A

prednisolone

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25
Q

Which cytokines exert an antiviral effect?

A

Interferons

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26
Q

Which Ig is a dimer?

A

IgA

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27
Q

Which cytokine acts on hepatocytes to induce synthesis of acute phase proteins in response to bacterial infection

A

IL6

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28
Q

What are the first immunoglobulins expressed on B cells before they undergo antibody class switching?

A

IgD and IgM

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29
Q

What is the most abundant (in terms of g/L) immunoglobulin in normal plasma?

A

IgG

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30
Q

Deficiency in which pathway predisposes to SLE?

A

Classical complement pathway

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31
Q

X-Linked Agammaglobulinaemia is due to a problem in which gene?

A

Bruton’s tyrosine kinase (Btk) gene

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32
Q

X-linked Severe Combined Immunodeficiency is due to a problem in which receptor?

A

IL2 receptor

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33
Q

Wiskott-Aldrich Syndrome is due to a problem in which gene?

A

WASP

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34
Q

Bare lymphocyte syndrome type 2 is due to a problem in which part of the immune system?

A

MHC class II

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35
Q

For which disorder would a bone marrow transplant be unhelpful but a thymic transplant may provide a cure?

A

DiGeorge syndrome

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36
Q

In acute rejection what is released by CD8 lymphocytes to kill target cells?

A

Granzyme B

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37
Q

What is a risk factor for chronic allograft rejection?

A

HTN

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38
Q

What are the 3 most important HLA types to screen for in renal transplantation when matching donor and recipient, in order of importance

A

HLA DR > B > A

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39
Q

Which lymphocytes respond to foreign HLA DR types

A

CD4+ T cells

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40
Q

Which lymphocytes respond to foreign HLA DR types

A

CD8+ T cells

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41
Q

Which immunosuppressant drug prevents DNA replication especially of T cells by impairing guanine synthesis

A

Mycophenolate mofetil

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42
Q

Which immunosuppressant drug causes a transient rise in neutrophils?

A

Prednisolone

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43
Q

SE of prednisolone?

A

HTN

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44
Q

SE of ciclosporin?

A

Hypertension and reduced GFR

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45
Q

SE of azathioprine?

A

Bone marrow depression
Hepatotoxicity
Hypersensitivity reactions

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46
Q

SE of methotrexate?

A

Pneumonitis, pulmonary fibrosis and cirrhosis

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47
Q

SE of immunoglobulin?

A

Anaphylaxis

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48
Q

Give an example of A sub-unit / conjugate vaccine

A

pneumococcal vaccine

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49
Q

What type of vaccine is oral poliomyelitis vaccine?

A

A live attenuated viral vaccine

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50
Q

Give an example of Inactivated preparations of the bacteria for vaccine

A

Whole cell typhoid vaccine

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51
Q

Give an example of a vaccine that is made using recombinant DNA technology

A

Hep B

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52
Q

Name a A feature of immunological central memory

A

IL2

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53
Q

Which live attenuated organism do BCG vaccines contain?

A

Mycobacterium bovis

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54
Q

What type of vaccine is HiB?

A

Conjugated

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55
Q

What Agent is used in humans that promotes a predominantly antibody response through the release of Il-4 that primes naïve B-cells?

A

Alum

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56
Q

What Diploid cell vaccine containing inactivated virus is given before or after exposure to those considered at risk?

A

Rabies

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57
Q

What type of vaccine is Hep A?

A

Inactivated

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58
Q

What is a A water-in-oil emulsion containing mycobacterial cell wall components that could be used to increase the immune response of a vaccine?

A

Freund’s adjuvant

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59
Q

What monoclonal antibody targets RANKL?

A

Denosumab

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60
Q

What drug class does dolutegravir belong to?

A

Integrase Inhibitor

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61
Q

The paediatric SpR is called to review a 21 day old infant who is pyrexic and appears unwell. He is noted to be hypocalcaemic and has a cleft palate. He has a fever of 39C. Blood tests reveal a neutrophil count of 8 (normal range: 1.5-8.0), absent T cells and normal B cells. What primary immunodeficiency is this patient likely to have?

A

DiGeorge Syndrome

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62
Q

What is the primary target of the antibody C-ANCA in Wegener’s?

A

Proteinase 3

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63
Q

What is the primary target of the antibody p-ANCA?

A

Myeloperoxidase

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64
Q

A patient’s autoimmune panel of bloods reveals positive anti-glycoprotein IIb antibodies. On the patient’s lower legs, there are pinprick petechiae. The patient’s platelet level is very low. What autoimmune condition is associated with this autoantibody and clinical presentation?

A

Autoimmune Thrombocytopenic Purpura

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65
Q

Encapsulated bacteria NHS?

A

Neisseria
Haemophilus
Streptococcus/Pneumococcus

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66
Q

What monoclonal antibody targets IL-17 and is involved in the treatment of psoriasis, psoriatic arthritis and ankylosing spondylitis?

A

Secukinumab

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67
Q

What immunoglobulin mediates type I hypersensitivity reactions?

A

IgE

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68
Q

What is the causative agent of Progressive Multifocal Leukoencephalopathy?

A

JC virus

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69
Q

A 5 year old girl is seen by her GP. Her mother says she is unable to sleep at night as her knees, elbows and shoulders are very red and painful, especially to touch. Her mother has also noticed small bumps under her skin. She is currently pyrexic, but the mother says she is still recovering from a bad sore throat two weeks ago.
What is the likely diagnosis?

A

Acute Rheumatic Fever

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70
Q

What is the short-term treatment for severe, life threatening antibody mediated damage or dysfunction, for example myasthenic crisis, cyroglobulinaemia or antibody mediated rejection?

A

Plasmapheresis

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71
Q

What lymphocyte lineage does azathioprine predominantly inhibit?

A

T lymphocytes

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72
Q

What assay is used as the gold-standard for diagnosis of HIV or as a confirmatory test of infection?

A

western blot

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73
Q

A 74 year old woman presents to the GP with of loss of vision and a severe headache around the sides of their head. In addition, she reports feeling generally tired and has trouble “getting going” in the morning.
An urgent referral to A&E is made. She treated urgently by the team and is admitted to hospital after blood results showed an elevated CRP. 24 hours after admission, a new set of bloods showed a moderate leukocytosis, which was not present on the previous bloods. In the absence of other symptoms, what is the most likely cause of the leukocytosis?

A

Corticosteroids

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74
Q

Which cell type secretes immunoglobulins?

A

Plasma cells

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75
Q

What is measured during an anaphylactic reaction to monitor response to treatment?

A

Mast Cell Tryptase

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76
Q

What viral enzyme is predominantly responsible for the high mutation rate of HIV and other RNA viruses?

A

Reverse Transcriptase

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77
Q

What specific cell subtype expresses both CD3 and CD4?

A

T Helper cells

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78
Q

What blood product is most commonly contaminated by bacteria?

A

Platelets

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79
Q

A 31 year old accountant reports an itchy rash over the trunk and back that has been present for the last 7 weeks. On examination, there are smooth erythematous papules with evidence of excoriation. She reports no association with food, time and has changed her washing powder to a “Non-Bio” formulation.
What condition is she suffering from?

A

Chronic Urticaria

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80
Q

What cell type is the hallmark of acute inflammation?

A

Neutrophils

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81
Q

What is the name given to a substance that increases the effectiveness of an immune reponse to a vaccination without altering the specificity of the response?

A

Adjuvant

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82
Q

A 70 year old gentleman is referred to the nephrologists for worsening kidney failure and haematuria. Over the last 3 months, he has lost 20% of his body weight, reports intermittent fevers and joint aches. He is also seeing his GP as he recently started coughing blood.
What underlying immunological condition may this patient have?

A

Goodpasture’s Disease

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83
Q

What is the inheritance pattern of reticular dysgenesis?

A

Autosomal recessive

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84
Q

An autoimmune panel of bloods reveals positive anti-dsDNA antibody at a titre of 1:1600.
What autoimmune condition is associated with this autoantibody?

A

SLE

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85
Q

Name 4 drugs which target TNF alpha

A

Infliximab
Adalimumab
Certolizumab
Golimumab

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86
Q

What is the only lymphocyte subset considered to be part of the innate immune system?

A

Natural killer cells

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87
Q

A 38 year old lady with known polycystic kidney disease received 3 units of blood over the last day due to a post-partum haemorrhage. She is complaining of shortness of breath. On examination she has mild pitting oedema of the sacrum and lower limbs. Serum BNP is elevated. She is apyrexic. What complication of blood transfusion is she suffering from?

A

Transfusion Associated Circulatory Overload

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88
Q

IgE antibodies bind semi-permanently to the surface of what cell of the innate immune system?

A

Mast cells

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89
Q

The paediatric SpR is called to review a 21 day old infant who is pyrexic and appears unwell. The parents think he has a problem with his hearing as he has been tugging at his ear. There is pain, tenderness and swelling over the mastoid process of his left ear. Blood tests reveal a neutrophil count of 0.1 (normal range: 1.5-8.0) What primary immunodeficiency is this patient likely to have?

A

Kostmann Syndrome

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90
Q

A 21 year old woman reports weight loss, tiredness, diarrhoea and non-bloody offensive smelling stools. She has had three chest infections requiring antibiotics in the last three years. Blood tests are ordered and reveals a hypochromic, microcytic anaemia with low ferritin. Anti-TTG and anti-endomysial antibodies are negative. There are normal levels of IgG, IgM and IgE. No IgA is found.
What is the most likely cause of her gastrointestinal symptoms?

A

Coeliac Disease

Anti-endomysial and anti-TTG are IgA autoantibodies so may be falsely negative in IgA deficiency

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91
Q

What does a correctable/reversible deformity of something like swan neck deformity in the hands suggest?

A

Suggests Jaccoud’s arthropathy as part of SLE rather than a diagnosis of rheumatoid arthritis

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92
Q

An arterial biopsy of a patient with a suspected arteritis reveals a “rosary bead” appearance of small aneurysms.
What vasculitis is associated with this clinical sign?

A

Polyarteritis Nodosa

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93
Q

An autoimmune panel of bloods reveals positive anti-liver kidney microsomal-1 antibody and anti-smooth muscle antibody. There is also derangement of LFTs. What autoimmune condition is associated with these autoantibodies and deranged LFTs?

A

Autoimmune Hepatitis

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94
Q

Which cytokine is predominantly responsible for T cell proliferation and survival?

A

IL2

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95
Q

Triad in Granulomatosis with Polyangitis?

A

Rapidly progressive glomerulonephritis
nosebleeds
haemoptysis

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96
Q

What is the most severe form of scid?

A

Reticular dysgenesis

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97
Q

What intracellular pro-proliferative molecule does cyclosporine and tacrolimus inhibit? What cytokine does this prevent release of?

A

Calcineurin

IL2

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98
Q

What is the specific antigen recognised by the immune system in Goodpasture’s syndrome?

A

Type IV collagen

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99
Q

What type of bacteria are conjugated vaccines effective against?

A

Encapsulated

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100
Q

A neutrophil releases preformed myeloperoxidase, defensins and neutrophil elastase. What is this process known as?

A

Degranulation

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101
Q

Prior to starting terbinafine, a systemic antifungal, what blood test should be ordered?

A

LFTs

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102
Q

Tx for Q fever?

A

Doxycycline or ciprofloxacin

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103
Q

Preggers and UTI?

A

nitrofurantoin

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104
Q

A 50 year old woman is seen by her GP with 3 days of mild headache, sneezing and coughing. She also has a sore throat. She takes ramipril for hypertension but has no other past medical history. On examination her chest is clear, there is no cervical lymphadenopathy and no visible exudate on the tonsils. What is the likely responsible organism?

A

Rhinovirus

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105
Q

What family of virus does dengue virus belong to?

A

Flavivirus

106
Q

Other than T lymphocytes, what cell type is primarily infected by HIV?

A

Macrophages

107
Q

What other 2 diseases should patients newly diagnosed with T1DM be screened for?

A

Coeliac

Hypo/hyperthyroidism

108
Q

What type of vaccine uses antigenic proteins to induce immunity?

A

Subunit (recombinant)

109
Q

What is the maximum number of viral capsids that a molecule of IgG may bind to?

A

2

110
Q

An autoimmune panel of bloods reveals a positive anti-centromere antibody. What autoimmune condition is associated with this autoantibody?

A

Limited Systemic Sclerosis

111
Q

What do you measure in a mantoux test?

A

Diameter of induration

112
Q

What monoclonal antibody targets IL-23 and IL-12 and is used in the treatment of psoriasis or psoriatic arthritis?

A

Ustekinumab

113
Q

Which cytokine is important in the pathogenesis of rheumatoid arthritis, anyklosing spondylitis and inflammatory bowel disease?

A

Tumour Necrosis Factor Alpha

114
Q

What HLA allele is associated with Systemic Lupus Erythematosus?

A

HLA-DR3

115
Q

Where are IgA antibodies typically found in the body?

A

Mucosal surfaces

116
Q

Autoantibodies directed against Fibrillarin and Scl70 are classically associated with what autoimmune condition?

A

Diffuse Cutaneous Systemic Sclerosis

117
Q

In haemolytic disease of the newborn, what maternal class of immunoglobulin is responsible for destruction of neonatal erythrocytes?

A

IgG

118
Q

What is the maximum number of viral capsids that a molecule of secretory IgA may bind to?

A

4

119
Q

What class of medication acts by inhibiting phospholipase A2 and reduces the expression of pro-inflammatory cytokines?

A

Corticosteroids

120
Q

What serine protease released by neutrophils causes hepatitis and emphysema in patients deficient in alpha-1 antitrypsin?

A

Neutrophil elastase

121
Q

List 6 type 2 hypersensitivity diseases

A

Pernicious anaemia (anti parietal cell antibodies)
Graves’ disease (anti-TSH receptor)
ITP (anti-platelet antibodies such as anti-glyoprotein IIb/IIIa)
Goodpasture’s syndrome (Anti-GBM antibodies [specifically anti-type IV collagen antibodies])
Haemolytic disease of the newborn (maternal IgG against fetal erythrocyte antigens)
Pemphigus Vulgaris (anti-cadherin)

122
Q

Which interleukins are classically responsible for inducing fever?

A

IL-1 and IL-6

123
Q

Which type of immunoglobulin is highly specific and is produced more than 5 days after an inital infection?

A

IgG

124
Q

2 examples of NRTIs?

A

Zidovudine

Abacavir

125
Q

Example of NNRTI?

A

Efavirenz

126
Q

Example of protease inhibitor?

A

Ritonavir

127
Q

Example of integrase inhibitor?

A

Dolutegravir

128
Q

What primary immunodeficiency is suggested in a patient with recurrent infections with E Coli, Staphylococcus Aureus, Listeria spp, Klebiella spp, Serratia marcescens and Candida species?

A

Chronic Granulomatous Disease

129
Q

What immune cell releases granzyme and perforin when activated?

A

CD8+ T cell

130
Q

What is the target of the autoantibodies responsible for pemphigus vulgaris?

A

Cadherin

131
Q

What test can be used to measure the levels of serum IgE directed against brazil nut antigens?

A

Radioallergosorbent test

132
Q

Which arm of the complement pathway is implicated in the pathogenesis of systemic lupus erythematosus?

A

Classical

133
Q

What autoantibody is associated with Granulomatosis with Polyangiitis (Wegner’s Granulomatosis)?

A

c-ANCA

134
Q

What gene is defective in Bruton’s agammagobulinaemia?

A

BTK gene

135
Q

Immunoglobulins may bind to multiple pathogens at once in order to enhance phagocytosis.
What is this process known as?

A

Agglutination

136
Q

What autoimmune condition is associated with AMA?

A

PBC

137
Q

Which subtype of T helper cells are implicated in the development of allergic diseases, such as asthma or eczema?

A

Th2

138
Q

What monoclonal antibody targets the IL-6 receptor and is involved in the treatment of rheumatoid arthritis?

A

Tocilizumab

139
Q

What monoclonal antibody targets alpha4 integrin and is used in the treatment of relapsing remitting multiple sclerosis?

A

Natalizumab

140
Q

What monoclonal antibody targets IL2a-receptor (CD25) and is used in the prophylaxis and treatment of allograft rejection? How does it do this?

A

Basiliximab

Reduces T cell proliferation

141
Q

What antigen does the immune system erroneously target in autoimmune thrombocytopenic purpura?

A

Glycoprotein IIb/IIIa

142
Q

What drug is given prophylactically to infants at high risk of developing life threatening RSV infection?

A

Palivizumab

143
Q

What is the maximum number of viral capsids that a molecule of IgM may bind to?

A

10

144
Q

What is the minimum number of Fc receptors on the surface of mast cells that must bind to an antigen to cause mast cell degranulation?

A

2

145
Q

What lymphocyte lineage does cyclophosphamide predominantly inhibit?

A

B cells

146
Q

A woman is undergoing investigation for a suspected primary immunodeficiency. An initial blood test revealed a markedly low neutrophil count. However, a repeat blood test two weeks later was normal. What primary immunodeficiency is this patient likely to have?

A

Cyclic neutropenia

147
Q

What hematological cells create a “respiratory burst” in order to kill phagocytosed pathogens?

A

Neutrophils

148
Q

What primary immunodeficiency is a patient with a negative dihydrorhodamine (DHR) test likely to have?

A

Chronic granulomatous disease

149
Q

What autoantibody is associated with Microscopic Polyangitis?

A

P-ANCA

150
Q

CD19 is typically a marker of what immune cell?

A

B cell

151
Q

An alcoholic patient presents to their GP for the first time following years of excessive drinking and poor self care.
The GP undertakes a number of investigations, including a blood film. What neutrophil abnormality would you expect to see?

A

Hypersegmented

152
Q

Describe febrile non-haemolytic reaction to whole blood products and why it occurs.

A

Symptoms include a fever >38 in mild cases or a high fever >39 with chills and rigors in severe reactions
Caused by white blood cells releasing cytokines such as IL-1 during storage

153
Q

How do you treat febrile non-haemolytic reaction to whole blood products?

A

Paracetamol

154
Q

In skin prick testing, what is used as a positive control?

A

Histamine

155
Q

An ANA test using indirect immunofluorescence suggests a homogenous pattern of ANA staining. What autoantibody is this pattern of ANA staining associated with?

A

anti-dsDNA

156
Q

An ANA test using indirect immunofluorescence suggests a speckled pattern of ANA staining. What autoantibody is this pattern of ANA staining associated with?

A

anti-centromere antibodies

157
Q

Diagnostic criteria of Common Variable Immunodeficiency? (3)

A

Decrease in serum IgG and a decrease in one of IgM or IgA
There is a lack of antibody response to antigens or immunisation
More than 4 years old

158
Q

Treatment of common variable immunodeficiency?

A

IVIG for life

159
Q

What is the gold-standard test for diagnosis of food allergy?

A

Double Blind Oral Food Challenge

160
Q

What specific malignancy are people with Sjogren’s syndrome at greater risk of?

A

Mucosa Associated Lymphoid Tissue Lymphoma

161
Q

CD14 is typically a marker of what type of immune cell?

A

Monocytes

162
Q

What immunoglobulin subtype binds to Fc receptors on the surface of mast cells?

A

IgE

163
Q

What type of hypersensitivity reaction is Type 1 Diabetes?

A

Type IV

164
Q

What auto-antibody is associated with Eosinophilic Granulomatosis with Polyangiitis (Churg Strauss)?

A

p-ANCA

165
Q

A 15 day old infant is brought to A&E by their concerned parents. He has been feeding poorly (<80% of normal) and is producing fewer wet nappies. He is quite sleepy.
On examination there are multiple discharging abscesses approximately half a centimeter in diameter visible around his umbilical cord stump. They are swollen and very red. The child’s father says his dad has a problem with white blood cells and takes injections for it. He is unsure what it is. The child is pyrexial at 38c and has a heart rate of 150bpm. A full blood count reveals a low neutrophil count. He was born at full term. What primary immunodeficiency is this child likely to have?

A

Kostmann Syndrome

166
Q

A severe asthmatic presents to their GP for the third time in three years complaining of blocked sinuses. However, over the last 6 months, she has also had unintentional weight loss and reports intermittent fevers. She also has an indistinct erythematous macular rash on both her ankles. A Full Blood Count reveals an eosinophilia (>10% of white blood cells). What rare immunological condition may be responsible for her symptoms?

A

Eosinophilic Granulomatosis with Polyangiitis

167
Q

A tumour cell has mutated and no longer expresses endogenous peptides and MHC Class I on the surface. What immune cell would recognise and kill this mutated cell?

A

Natural Killer cells

168
Q

What is the most common inherited primary immunodeficiency?

A

Selective IgA Deficiency

169
Q

A 34 year old man has severe Crohn’s disease. His gastroenterologist wishes to start an anti-TNF drug to see if it controls his symptoms better. What first-line test should the patient undergo before starting adalimumab?

A

Mantoux Test

170
Q

A 31 year old woman presents to their GP with tiredness and offensive smelling diarrhoea but no blood. Since the diarrhoea has started, she has complained of recurrent bouts of skin infections and food poisoning like symptoms. She is anti-TTG and anti-endomyseasal antibody positive. A full STI screen is negative. FBC is unremarkable. Albumin and Immunoglobulins are low. What is the reason for her recurrent infections?

A

Protein losing enteropathy

171
Q

How do you diagnose a protein losing enteropathy?

A

faecal alpha-1 antitrypsin levels

172
Q

An autoimmune panel of bloods reveals positive anti-Jo-1 antibody in a woman with breast cancer. What autoimmune condition is associated with this autoantibody?

A

Dermatomyositis

173
Q

Which type of immunoglobulin is primarily secreted into breast milk and is responsible for passive immunity in newborns?

A

IgA

174
Q

Immunoglobulins may bind to bacteria to allow phagocytosis to occur. What is this process known as?

A

Opsonisation

175
Q

What enzyme, deficient or defective in chronic granulomatous disease, is responsible for the “respiratory burst” that may kill phagocytosed pathogens?

A

NADPH oxidase

176
Q

Immunoglobulins may bind to cell surface receptors on viruses, to prevent viral binding and entry of human cells.
What is this function of immunoglobulins known as?

A

Neutralisation

177
Q

What CD number do T reg cells have on their surface and what transcription factor do they express?

A

FOXP3

CD25

178
Q

What protein is defective in X linked Severe Combined Immunodeficiency?

A

Common Gamma Chain

179
Q

An prenatal autoimmune panel of bloods reveals positive anti-Ro antibody in the blood of a pregnant woman with SLE. What cardiological condition is her unborn baby at risk of?

A

Congenital Heart Block

180
Q

A 33 year old man is seen by the rheumatologists for evaluation of his raynaud’s syndrome. He says his hands are becoming more sensitive to changes in temperature. In addition, the skin is cracked and dry. During the appointment, he is constantly sipping water from a water bottle. An autoimmune antibody screen reveals positive ANA (Anti-Ro, Anti-La positive). What autoimmune condition explains his symptoms?

A

Sjogren’s Syndrome

181
Q

What immunomodulatory agent may be given to treat chronic granulomatous disease?

A

Interferon Gamma

182
Q

A 10 year old has severe hayfever. Twice in the last month she has complained to her parents of tingly lips after eating celery. She also says the same thing happens when she eats apples. What allergic condition is the cause of her symptoms?

A

Oral Allergy Syndrome

183
Q

A mutation in what protein is the most common cause of Hyper IgM syndrome?

A

CD40 ligand

184
Q

What monoclonal antibody targets CD52 and causes depletion of all lymphocyte subsets?

A

Alemtuzumab

185
Q

Congenital absence of C4 (Complement) predisposes to what autoimmune disease?

A

SLE

Also absence of C2 or C3

186
Q

How may mast cell degranulation be measured?

A

Tryptase

187
Q

What are the pathogenic antibodies in bullous pemphigoid?

A

Anti-Hemidesmosome

188
Q

Mutation in what cell surface receptor may confer immunity from HIV?

A

CCR5

189
Q

Clinical symptoms of Eosinophilic Granulomatosis with Polyangiitis?

A

Patients affected typically have severe allergies or sinus problems, which progress to severe asthma prior to the systemic vasculitis.

190
Q

Clinical features of SCID?

A

Recurrent infections
Diarrhoea
Failure to thrive
Skin disease

191
Q

Autosomal recessive SCID is caused by a mutation in which gene?

A

Adenosine deaminase

192
Q

Causes of protein losing enteropathy?

A

Crohn’s
Coeliac
Menetrier’s disease

193
Q

Where is the mutation in cyclic neutropenia and what is the inheritance?

A

Neutrophil elastase gene (ELA2)

AD

194
Q

Features of Wiskott-Aldrich syndrome?

A

Lymphoma
Thrombocytopenia - easy bruising, nose bleeds, GI bleeds
Eczema
Recurrent bacterial infections

195
Q

Blood test results for Wiskott-Aldrich syndrome (in terms of Ig)

A

Decreased IgM
Raised IgA and IgE
Variable IgG

196
Q

Where is the mutation in CVID and what does it cause?

A
MHC III
Causes aberrant class switching - leads to infection with H. influenzae and Strep pneumoniae
197
Q

When does CVID present?

A

In adulthood

198
Q

What happens in bare lymphocyte syndrome type 1 and 2

A

Type 1: MHC Class I deficiency - all T cells become CD4+

Type 2: MHC Class II deficiency - all T cells become CD8+

199
Q

Clinical features of bare lymphocyte syndrome?

A

Sclerosing cholangitis
Hepatomegaly
Jaundice

200
Q

What is the role of IgA?

A

Provides mucosal immunity mainly to respiratory and GI system

201
Q

Clinical features of selective IgA deficiency?

A

Recurrent Mild respiratory and GI infections

202
Q

What does deficiency in common pathway of complement predispose you to?

A

Infection with encapsulated bacteria

203
Q

What does deficiency in interferon gamma receptor predispose you to?

A

Intracellular infection e.g. TB and salmonella

204
Q

What monoclonal mouse ab used to be used to prevent allograft rejection and what did it bind to?

A

Muromonab (OKT3)

CD3

205
Q

What is Felty’s syndrome?

A
Extra-articular manifestations of RA:
Pulmonary fibrosis
Pericardial effusion
Rheumatoid nodules
Splenomegaly
206
Q

What Ab is seen in dermatomyositis?

A

Anti-Jo1

207
Q

Clinical features of dermatomyositis?

A

Heliotrope rash
Gottron’s papules
Proximal myopathy
Pulmonary fibrosis

208
Q

What type of hypersensitivity reaction is extrinsic allergic alveolitis?

A

Type III

209
Q

What type of hypersensitivity reaction is AIHA?

A

Type II

210
Q

Triggers of AIHA?

A
Idiopathic
SLE
CLL
Methyldopa
Penicillin
211
Q

What type of hypersensitivity reaction is polyarteritis nodosa?

A

Type III

212
Q

What investigation results would you expect to see in polyarteritis nodosa?

A

Raised CRP, ESR and Ig
p-ANCA
Multiple aneurysms

213
Q

What hypersensitivity reaction is occuring in ITP and what is it directed at?

A

Type 2

IgG targets GlpIIb-IIIa

214
Q

What foods are associated with oral allergy syndrome?

A

Stony fruits

215
Q

SE of cyclophosphamide?

A

Bone marrow suppression
Hair loss
Bladder cancer

216
Q

Indications for cyclophosphamide therapy?

A

SLE
connective tissue disease
vasculitis (Wegener’s)

217
Q

What is abatacept and what is it used to treat?

A

CTLA-4-immunoglobulin fusion protein

RA

218
Q

SE of abatacept?

A

Infection from TB, HBV, HCV

219
Q

MOA of abatacept?

A

Binds to CD80 and CD86 on surface of APCs and prevents APCs from delivering co-stimulatory molecule to T cells to activate them

220
Q

SE of Mycophenolate mofetil?

A

Bone marrow suppression

HSV reactivation

221
Q

What does efalizumab bind to and what does this cause? What is it used to treat?

A

CD11a on T cells
Inhibits T cell migration
Psoriasis

222
Q

What does ustekinumab bind to and what does this cause? What is it used to treat?

A

IL12 and IL23
Prevents T cell and NK cell activation
Psoriatic arthritis

223
Q

Triad in wegener’s?

A

Epistaxis
Haemoptysis
Haematuria

224
Q

When does IgA nephropathy occur?

A

After GI or URTI

225
Q

What are the 3 types of rapidly progressive glomerulonephritis and what is seen on IgG/C3 immunofluorescence?

A

Immune complex disease - granular staining
Pauci-immune disease - absent/scant staining
Anti-GBM disease - linear staining

226
Q

What is there activation of in membranoproliferative glomerulonephritis?

A

Classical and alternative complement pathway

227
Q

What test is used to detect sarcoidosis?

A

Kveim test

Injection of spleen from known sarcoid patient followed by non-caseating granuloma formation 4-6 weeks later

228
Q

What does a high CH50 indicate?

A

Acute or chronic inflammation

229
Q

Features of APECED?

A
Mild immune deficiency
Dysfunctional parathyroid + adrenal
Hypothyroid
Gonadal failure
Alopecia
Vitiligo
230
Q

Pathological mechanism of post-step rheumatic fever?

A

Molecular mimicry

231
Q

Mechanism of mycoplasma causing AIHA?

A

T cell bypass and modification of RBC surface antigens

232
Q

In SLE which falls first C3 or C4?

A

C4

233
Q

Which patients are blood transfusions contraindicated in?

A

SCID

234
Q

Clinical features of Bare lymphocyte syndrome?

A

Sclerosing cholangitis with hepatomegaly and jaundice

235
Q

What is WAS associated with?

A

Lymphoma (causes lymphopenia)
Thrombocytopenia
Eczema

236
Q

Release of which cytokine from T cells activates macrophages?

A

Interferon gamma

237
Q

What does IFN-g deficiency increase risk of?

A

Intracellular organism infection e.g. TB and salmonella

Since granulomas can’t form

238
Q

What infection are people with hyper IgM syndrome at risk of?

A

PCP infection

239
Q

Clinical features of CVID?

A

Bronchiectasis

Sinusitis

240
Q

In a type 2 hypersensitivity reaction what do IgG and IgM stimulate?

A

Classical complement pathway

241
Q

What do acantholytic cells on biopsy suggest?

Which antibody is involved?

A

Pemphigus vulgaris

Anti-demoglein

242
Q

Explain the steps of type 4 hypersensitivity

A
  1. APCs (macrophages) engulf antigen and present to CD4 which binds
  2. Macrophage then releases IL12 - making memory Th1 cells
  3. On second exposure to allergen macrophage presents it to CD4 cells
  4. Memory Th1 cells release IFNg, IL2 and IL3
  5. These cytokines activate TNF-a production by macrophages
243
Q

Proteins involved in MS?

A

Myelin basic protein

Proteolipid protein

244
Q

Define isograft

A

From identical twin

245
Q

When does acute cellular rejection occur after transplant?

A

1 week after

246
Q

When does acute vascular rejection occur after transplant? With which type of graft?

A

4-6 days after

Xenograft

247
Q

Daclizumab? Used for what?

A
IL2 antibody (CD25)
Kidney transplant to prevent rejection
248
Q

What is interferon alpha used to treat?

A

Hep B
Hep C
Kaposi’s sarcoma
CML

249
Q

What is interferon beta used to treat?

A

MS

250
Q

What is interferon gamma used to treat?

A

chronic granulomatous disease

251
Q

What does homogenous staining on immunofluorescence suggest?

A

Anti-histone: drug induced SLE

252
Q

What does nucleolar staining on immunofluorescence suggest?

A

Anti-RNA polymerase: systemic sclerosis

253
Q

What does peripheral staining on immunofluorescence suggest?

A

Anti-dsDNA: SLE

254
Q

What does speckled staining on immunofluorescence suggest?

A

Anti-Jo: dermatomyositis
Anti-Smith: SLE
Anti-RNP: mixed connective tissue disease
Anti-Ro: Sjogren’s

255
Q

What causes the fibrosis in limited systemic sclerosis?

A

TNF-beta

256
Q

Features of Kearns-Sayre syndrome?

A
Ptosis and difficulty with eye movement
Pigmentary retinopathy
Proximal muscle weakness
Cardiac conduction defects
Hearing loss
Cerebellar ataxia
Endocrine: hypoparathyroid, hypogonad, DM, hypopituitary
257
Q

Features of IPEX?

A

DM
Eczema
Enteropathy

258
Q

Biopsy findings of autoimmune hep?

A

Interface hepatitis

259
Q

Autoimmune hep type 1 vs 2?

A

Type 1: Adults, anti-SMA, ANA

Type 2: kids, anti-LKM, steroid resistant, associated with IgA deficiency

260
Q

What is seen on immunofluorescence of focal segmental glomerulonephritis?

A

IgM and C3 deposition

261
Q

What is seen on immunofluorescence of membranous glomerulonephritis? Also post-strep glomerulonephritis

A

Sub-epithelial granular deposits of IgG and C3

262
Q

Most abundant immunoglobulin in breast milk?

A

IgA