4 Flashcards
1
Q
List 5 signs of anaemia
A
Signs: pallor, tachycardia, glossitis, koilonychia, dark urine
2
Q
List 4 symptoms of anaemia
A
Symptoms: weakness, SoB, palpitations, fatigue
3
Q
What is glossitis?
A
Swollen, red, painful tongue (vitamin B12 deficiency)
4
Q
Koilonychia
A
Spoon nails (caused by iron deficiency)
5
Q
Tinnitus
A
A sensation of noise (such as a ringing or roaring) that is typically caused by a bodily condition.
6
Q
Role of vitamins B6 (folate) and B12 (cobalamin) in RBC production?
A
Deficiency of B6 or vitamin B12 inhibits purine and thymidylate syntheses, impairs DNA synthesis, and causes erythroblast apoptosis, resulting in anemia from ineffective erythropoiesis
7
Q
What are erythropoiesis?
A
Production of red blood cells
Erythropoietin (EPO) regulates erythropoiesis
8
Q
In what kind of anaemia is dark urine common?
A
Haemolytic anaemia
9
Q
Define haematopoiesis.
A
Formation of the cells of immune system + blood cells.
10
Q
What are haematopoietic stem cells (HSCs) + where do they reside?
A
Cells which can give rise to all the different blood cells.
In adults, under steady-state conditions, the majority of HSCs reside in bone marrow.
However, cytokine mobilization can result in the release of large numbers of HSCs into the blood.
As a clinical source of HSCs, mobilized peripheral blood (MPB) is now replacing bone marrow, as harvesting peripheral blood is easier for the donors than harvesting bone marrow.
11
Q
Why are HSCs known as being self-renewing?
A
They reside in the bone marrow + when they proliferate, at least some of their daughter cells remain as HSCs so stem cell pool is not depleted (asymmetric division).
12
Q
What is asymmetric division? Give an example.
A
Asymmetric cell division produces two daughter cells with different cellular fates. E.g. HSC proliferation.
13
Q
What are the daughter cells of HSCs? Can they renew themselves?
A
HSCs – can renew themselves
Myeloid progenitor cells – cannot renew themselves
Lymphoid progenitor cells – cannot renew themselves
14
Q
All blood cells are divided into which 2 lineages?
A
Lymphoid progenitor cells and Myeloid progenitor cells
15
Q
What do myeloid progenitor cells divide into?
A
Erythrocyte
Megakaryocyte (> Thrombocyte)
Mast cell
Myeloblast:
- Granulocytes: Neutrophil, Eosinophil, Basophil
- Monocyte (> Macrophage)
16
Q
What do lymphoid progenitor cells divide into?
A
Small lymphocytes:
- T cells
- B cells (> Plasma cells)
Large granular lymphocyte:
- Natural killer cells
17
Q
What is a proerythroblast?
A
A precursor cells that will eventually become a RBC
18
Q
Which vitamin are essential for DNA synthesis?
A
Vitamin B12
Vitamin B9 (folate)
Vitamin B6
19
Q
What 2 things cause anaemia?
A
Reduced production of functional erythrocytes or production of defective haemoglobin.
Increased destruction of erythrocytes.
20
Q
List 3 essential micronutrients that are critical in the production of erythrocytes and haem synthesis.
A
Vitamin B12 + B9 (folate)
Iron
21
Q
What do the abbreviations in a full blood count mean: MCV, HCT, MCH, MCHC, RDW?
A
MCV – mean corpuscular volume (RBC size)
HCT – haematocrit (PCV – proportion of RBCs in blood)
MCH – mean corpuscular haemoglobin (average amount of haemoglobin in RBCs)
MCHC – MCH concentration (average % of haemoglobin in the RBCs)
RDW – red blood cell distribution width
22
Q
List complications of SCA?
A
Vaso-occlusive crises
Visceral sequestration crisis
Haemolytic crises
Stroke
Hyposplenism
Ulcers
23
Q
Which receptors do IgE antibodies bind to on mast cells?
A
FcεRI on mast cell where the Fc region of IgE binds to
24
Q
What is sideroblastic anaemia?
A
Form of anaemia in which the bone marrow produces ringed sideroblasts rather than healthy erythrocytes.
25
What is pancytopenia?
Conditions affecting production of other cell types in addition to RBCs.
26
What is PRCA pure red cell aplasia?
Conditions affecting specifically erythropoiesis in the bone marrow.
27
What leads to pancytopenia?
Failure of HSCs to self-renew eventually leads to HSC exhaustion and pancytopenia.
28
What is haemolytic anaemia?
Premature destruction of functional erythrocytes by intrinsic or extrinsic mechanisms.
29
What are the 2 reasons why erythrocyte destruction usually occurs (extrinsic and; intrinsic)?
1. Nothing wrong w/ the erythrocyte but they are destroyed by external pathological processes such as drugs, toxins, auto-antibodies or infection.
2. Something intrinsically wrong w/ the erythrocyte so it’s destroyed. E.g. abnormal Hb, lacks certain enzymes
30
What is SCA caused by?
Mutation in the beta-globin gene
31
What does a RBC get broken down into (in the spleen/liver/red bone marrow)?
Globin - aa - reused for protein synthesis
Heme - liver (bilirubin and ferritin) - excretion
32
What are haemoglobinopathies?
Give an example.
Hemoglobinopathies are inherited single-gene disorders; in most cases, they are inherited as autosomal co-dominant traits
E.g. SCA
33
What does SCA affect?
Due to abnormally shaped SC erythrocytes issues w/ passage through circulatory system and ability to carry O2
34
What is a splenic sequestration crisis?
Intrasplenic sickling prevents blood from leaving the spleen and acute splenic engorgement ensues
35
What is a haemolytic crisis?
The rapid destruction of large numbers of red blood cells (haemolysis)
The destruction occurs much faster than the body can produce new red blood cells.
36
What is a vaso-occlusive crisis and its causes?
Sickle-shaped RBCs block blood vessels. Blood and oxygen cannot get to tissues, causing pain.
37
What characterises hypochromic and microcytic RBCs?
Hypochromic – pale RBCs
| Microcytic – small RBCs
38
What is sideroblastic anemia caused by and characterised by?
Characterised by failure to incorporate iron into haem in erythrocyte precursor cells.
Caused by mutations/deletions of genes regulating expression of key enzymes in haem synthesis.
39
Describe what happens to broken down heme components.
Heme -->
Biliverdin and Fe3+ -->
Bilirubin and Fe3+ (goes to liver) -->
Bilirubin secreted in bile into the SI where it become urobilinogen -->
Urobilin (urine) / stercobilin (faeces)
40
What is the role of transferrin in the breakdown of haemoglobin?
Carries Fe3+ in the blood from macrophage to liver and liver to red bone marrow.
41
What does bilirubin get broken down into in the kidney and large intestines?
Kidney – urobilin
| LI – stercobilin
42
What 2 components is heme broken down into?
Biliverdin and Fe3+
43
What happens to the globin broken down from RBCs?
Breaks down into amino acids and are reused for protein synthesis
44
Put these in order in starting from RBC being phagocytosed in liver, spleen, or red marrow: bilirubin, urobilinogen, biliverdin, urobilin.
Biliverdin, bilirubin, urobilinogen, urobilin
45
List the components of blood cells.
Erythrocytes, thrombocytes, leukocytes
46
List the components of blood plasma.
Water, proteins, inorganic ions, organic substances
47
What are the blood cells of the innate immune system?
Neutrophils, monocytes, basophils, eosinophils, mast cells, natural killer cells.
48
Type 1 hypersensitivity reactions are mediated by which type of antibody in humans?
IgE
49
In hypersplenism is MCV high, low or normal?
Normal
50
In liver disease is MCV high, low or normal?
High
51
In thalassemia is MCV high, low or normal?
Low
52
In iron-deficiency anaemia is MCV high, low or normal?
Low
53
What is the difference between sideroblastic anaemia and haemolytic anaemia?
Sideroblastic – Low MCV and few RBCs (failure of iron incorporated in Hb)
Haemolytic – Normal MCV (RBCs breakdown > formation)
54
What does the common lymphoid progenitor develop into?
T and B lymphocytes, NK cells, lymphoid dendritic cells.
55
Where to T cell develop and migrate to?
Develop in the thymus and migrate to spleen.
56
Where does the common myeloid progenitor develop?
In the red bone marrow and completes in lymphatic tissue
57
Name 3 granulocytes.
Eosinophil, basophil, neutrophil
58
Name all the agranulocytes (mononuclear).
Monocytes (macrophages, DC), lymphocytes (B and T cells)
59
What is the suffix of all granulocytes?
-phil
60
What is the suffix of most agranulocytes?
-cyte
61
What does a monocyte differentiate into and where?
Macrophage or dendritic cells when they migrate from bloodstream to tissues.
62
What does the B lymphocyte become once activated?
B effector cells.
63
What do megakaryocytes develop into?
Thrombocytes (platelets)
64
What is the bone marrow a site of?
Blood formation
65
How does haematopoiesis change as we develop and age?
Prenatal months – blood produced: yolk sac, liver, spleen
Postnatal years – bone marrow of tibia (0-20), femur (0-25), vertebrae and pelvis, sternum and ribs forever.
66
Where is most blood produced in prenatal foetuses?
Liver
67
CTLA-4 is an important negative regulator of T cell activation. How does it function?
Is a protein receptor that functions as an immune checkpoint, downregulates immune responses. Is expressed in Tregs.
68
In prenatal and postnatal years, what type of Hb is produced?
Prenatal – alpha and gamma
| Postnatal – alpha and beta
69
In postnatal years, over 25 where is blood produced?
Bone marrow of vertebrae, pelvis, sternum and ribs
70
What regulates haematopoiesis?
GFs including: IL-1,2,3,7, GM-CSF, G-CSR, M-CSF, TPO, EPO
71
Protein regulators that determine the fate of haematopoietic cells drive what?
Self-renewal, cell death, expansion and differentiation.
72
What does EPO, TPO and cytokines regulate formation of?
EPO – RBCs,
TPO – platelets,
Cytokines – WBCs
73
Bone marrow contains which distinct features?
```
Trabecular bone,
Granulocytes,
Megakaryocytes,
Erythroid islands,
Steatocytes
```
74
What are steatocytes?
Fat cells, they maintain metabolic state by storing energy needed for proliferation
75
What are erythroid islands?
Erythroblasts making erythrocytes
76
What are megakaryocytes?
A large bone marrow cell w/ a lobulated nucleus. It produces thrombocytes.
77
What is trabecular (spongy) bone? Where is it found?
a.k.a. cancellous bone. It is very porous and contains red bone marrow, where blood cells are made.
Found at ends of long bones, pelvic bones, ribs, skull and vertebrae (spinal).
78
What are granulocytes?
A white blood cell with secretory granules in its cytoplasm, e.g. an eosinophil or a basophil.
79
Immature blood cells initially interact with which type of cells in the marrow?
Stomal cells in the marrow.
80
Delta, epsilon and zeta chains are associated with what and when do they disappear?
The yolk sac, disappear v. early (9 weeks)
81
What is the point of having LT-HSC (long term haematopoietic stem cells?
They divide rarely so little chance of mutations/damage etc. so they last entire lifespan.
82
What do LT-HSC differentiate into?
LT-HSC, ST-HSC
83
What are MPPs (multipotent progenitor cells)?
Cells committed to either the lymphoid or myeloid lineages and give rise to more differentiated precursors.
84
Why is foetal haemoglobin different from adult haemoglobin?
Because it must bind oxygen at lower partial pressure (from mother) so it must have a higher affinity for oxygen than adult Hb
85
What is made in the bone marrow at a rate of 2.4 x 106 per second?
RBCs
86
What does gamma interferon induce?
Activation of macrophages and inducer of MHC class II expression
87
What is the key role of macrophages in the spleen?
Removal of damaged RBCs
88
What is the life span of RBCs?
120 days
89
95% of the blood in the body filters through the spleen in what time frame?
3 minutes
90
What is the straw-coloured liquid component of the blood called?
Blood plasma
91
Name the methods of analysis of blood.
Spectrometry and impedance, cytochemistry, flow, cytometry, immunoassays, microscopy.
92
What are the 3 plasma proteins and what synthesises them?
Albumins, globulins, fibrinogen
93
What are gamma globulins?
Plasma proteins, a.k.a. immunoglobulins (Ab)
94
What determines blood type?
Antigen A and B on surface of RBCs
95
What naturally occurring antibody type in the serum targets non-present ABO antigens?
IgM
96
Circulating platelets have a life span of what?
5-9 days
97
What controls the lifespan of circulating platelets?
Integral apoptotic regulating pathway
98
What 3 types of granules do platelets contain?
Dense – ADP, ATP, calcium ion, magnesium, serotonin
Lambda – hydrolytic enzymes
Alpha – PF-4, TGF-beta-1, vWF, fibrinogen (factor I), factor V, fibronectin
99
What does dense granules in platelets contain?
ADP, ATP, calcium ion, magnesium, serotonin
100
What does alpha granules in platelets contain?
PF-4, TGF-beta-1, vWF, fibrinogen (factor I), factor V, fibronectin
101
Platelet reserves in spleen can be released by what?
Splenic contraction
102
What does thrombopoietin regulate?
Formation of platelets
103
Platelets form from what of the megakaryocyte?
Cytoplasm
104
Each megakaryocyte releases how many platelets?
2000-5000
105
What does vWF do?
A blood glycoprotein involved in haemostasis.
106
What does fibrinogen do?
a.k.a factor I – is a blood plasma protein made in the liver.
It’s a coagulation factor responsible for normal clotting
107
What is myeloproliferative neoplasms?
Too much proliferation of myeloid cells
108
What is polycythemia vera?
Excess of RBCs in circulation
109
What is the difference between primary and secondary polycythemia?
1 – genetic problems in RBCs, e.g. PV, congenital/familial
2 – conditions promote RBC development, e.g. hypoxia, EPO secreting tumours, neonatal polycythemia.
110
What does EPO secreting tumours cause?
Too much EPO secretion which upregulates the production of erythrocytes --> secondary polycythaemia
111
What is relative polycythemia?
When RBCs are normal but reduced plasma volume e.g. dehydration is causing the problem.
112
What is essential thrombocythemia?
Excess platelets
113
What is myelofibrosis?
Primary myelofibrosis is a relatively rare bone marrow cancer. It is currently classified as a myeloproliferative neoplasm, in which the proliferation of an abnormal clone of hematopoietic stem cells in the bone marrow and other sites results in fibrosis, or the replacement of the marrow with scar tissue.
The term myelofibrosis alone usually refers to primary myelofibrosis (PMF), also known as chronic idiopathic myelofibrosis (cIMF);
- The terms idiopathic and primary mean that in these cases the disease is of unknown or spontaneous origin.
This is in contrast with myelofibrosis that develops secondary to polycythemia vera or essential thrombocythemia.
Myelofibrosis is a form of myeloid metaplasia, which refers to a change in cell type in the blood-forming tissue of the bone marrow, and often the two terms are used synonymously. The terms agnogenic myeloid metaplasia and myelofibrosis with myeloid metaplasia (MMM) were also used to refer to primary myelofibrosis.
114
Which JAK gene is involved in myeloproliferative neoplasms?
JAK-2;
Makes HSCs more sensitive to growth factors
115
What is parasitism?
One organism benefits at the expense of the other
116
What is mutualism?
Both organisms benefit
117
What is commensalism?
One organism benefits, the other is unaffected
118
From smallest to largest list all the pathogens.
Virus, intracellular bacteria, extracellular bacteria, archaea, protozoa, fungi, parasites
119
In what 3 ways does the innate immune system protect against pathogens?
Anatomical barriers
Complement/antimicrobial protein activation
Inflammation
120
Is the innate or adaptive immune response more efficient?
Adaptive due to high specificity of antigen recognition by its lymphocytes
121
What is complement?
Part of the innate immune system that enhances the ability of Ab and phagocytic cells to clear microbes and damaged cells from an organism.
Promotes inflammation and attacks pathogen’s plasma membrane. Consists of a number of small proteins syn by liver.
122
Many tissue-resistant macrophages arise when?
During embryonic development
123
List the granulocytes and agranulocytes
Granulocytes:
- Neutrophils
- Basophils
- Eosinophils
Agranulocytes:
- Monocytes (macrophages)
- Lymphocytes (T + B cells, NK cells)
124
Precursors of platelets (thrombocytes)?
Megakaryocytes -->
Pro-megakaryocyte -->
Megakaryoblast -->
Common myeloid progenitor -->
Hematopoietic stem cell
125
Microcytic anaemia causes
- Iron-deficiency anaemia
- Thalassaemia*
- Congenital sideroblastic anaemia
- Lead poisoning
*in beta-thalassaemia minor the microcytosis is often disproportionate to the anaemia
126
Normocytic anaemia causes
- Anaemia of chronic disease
- Chronic kidney disease
- Aplastic anaemia
- Haemolytic anaemia
127
Aplastic anaemia
Characterised by pancytopaenia and a hypoplastic bone marrow
Causes:
- Idiopathic
- Congenital: Fanconi anaemia, dyskeratosis congenita
- Drugs: cytotoxics, chloramphenicol, sulphonamides, phenytoin, gold
- Toxins: benzene
- Infections: parvovirus, hepatitis
- Radiation
Features:
- Normochromic, normocytic anaemia
- Leukopenia, with lymphocytes relatively spared
thrombocytopenia
- May be the presenting feature acute lymphoblastic or myeloid leukaemia
- Minority of patients later develop paroxysmal nocturnal haemoglobinuria or myelodysplasia
128
Macrocytic anaemia causes
Megaloblastic, macrocytic causes
- Vitamin B12 deficiency
- Folate (B9) deficiency
Normoblastic, macrocytic causes:
- Alcohol
- Liver disease
- Hypothyroidism
- Pregnancy
- Reticulocytosis (haemolytic anaemia)
- Myelodysplasia
- Drugs: cytotoxics
129
Haemoglobinopathies vs Thalassemias vs structural haemoglobin variants?
The hemoglobinopathies encompass all genetic diseases of hemoglobin.
They fall into two main groups: thalassemia syndromes and structural hemoglobin variants (abnormal hemoglobins). α- and β-thalassemia are the main types of thalassemia; the main structural hemoglobin variants are HbS, HbE and HbC.
130
Examples of structural haemoglobin variants
Sickle cell anaemia (HbS)
Congenital dyserythropoietic anemia
Many hemoglobin variants do not cause pathology or anemia, and thus are often not classed as hemoglobinopathies, because they are not considered pathologies.
131
Examples of thalassemias
There are two main types, alpha thalassemia and beta thalassemia.
The severity of alpha and beta thalassemia depends on how many of the four genes for alpha globin or two genes for beta globin are missing
132
Hereditary spherocytosis
Hereditary spherocytosis is an abnormality of erythrocytes.
Hereditary spherocytosis can be an autosomal recessive or autosomal dominant trait.
The disorder is caused by mutations in genes relating to membrane proteins that allow for the erythrocytes to change shape.
The abnormal erythrocytes are sphere-shaped (spherocytosis) rather than the normal biconcave disk shaped.
Leads to haemolytic anaemia due to spleen's function of removing dysfunctional RBCs.
