White Blood Cells Flashcards

1
Q

Granulocytes-Eosinophil, what do they fight

A

defence against parasites, regulation of hyper-sensitivity

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2
Q

Granulocytes- Basophils, what’s in their granules and what does this combat

A

it’s granules contain histamine, heparin and proteolytic enzymes. Vs hyper-sensitivity in which IgE-coated Basophils release histamines.

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3
Q

Granulocytes- Neutrophils, type of nucleus, mechanisms for phagocytosis

A

segmented nucleus, phagocytosis, chemotaxis, 2 mechanisms: super oxide dependent- release of reactive O2 species (respiratory burst) which gives substrate for myeloperoxidase, releasing toxic substance
OR O2 independent= variety of anti-microbial release

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4
Q

Monocytes and macrophages, what do they do and how are they linked

A
  1. chemotaxis, phagocytosis and antigen presentation for lymphoid cells. 2. phagocytosis and scavenging function, store and release iron
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5
Q

Lymphoid cells- T cells from Thymus, the 2 types and their roles

A

CD4=helper T, releases cytokines (IF) which increases synthesis of antibodies
CD8=cytotoxic T, destroys virus infected cells

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6
Q

Lymphoid cells- B cells, how they form varied immunoglobins and what they develop into

A

in fœtus gène réarrangement of immunoglobulin heavy and light chains= production of surface immunoglobulins vs antigens
Turn into antibody producing plasma cells

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7
Q

Lymphoid cells- Natural killer cells

A

innate, kill tumour and virus infected cells

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8
Q

Abnormalities- Neutrophilia, symptoms and causes

A

Symptoms- left shift, more non segmented neutrophils, more neutrophil precursors
Causes- infection, inflammation, myeloproliferative disorders eg CML, pregnancy, post exercise

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9
Q

Abnormality- Neutropenia, symptoms and causes

A

chemo/radiotherapy, autoimmune, severe infections, benign ethnic neutropenia in africans, hypersegmentation due to lack of B12/folate

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10
Q

Abnormality- Lymphocytosis, example of it in kids, discuss the two types of leukaemia this is present it

A

response to virus, whooping cough in kids, chronic lymphocytic leukaemia shown by smudge/smear lymphocytes, atypical lymphocytes (more lobed) acute lymphoblastic leukaemia= more lymphoblasts which dont mature into lymphocytes, impairing haemopoiesis, lymphoblasts circulate in blood. Acute conditions are severe and sudden, for treatment give RBC, platelets, antibiotics and chemo

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11
Q

Chronic myeloid leukaemia, discuss how and why, and cures

A

ABL 1 gêne encodes tyrosine kinase, BCR on chrom22 swaps with ABL1, therefore ABL1-BCR encodes protein with uncontrolled tyrosine kinase=leukaemia clone, abnormally short chrom22=Ph chrom, symptoms=splénomégaly, cure= tyrosine kinase inhib

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