Platelets and HLA Flashcards

1
Q

What are the two main types of platelet products?

A

Apheresis platelets (single donor) and pooled platelets (from 7 buffy coats).

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2
Q

How are pooled platelets prepared?

A

7 ABO-matched buffy coats are combined with PAS-E, leukoreduced, and pathogen-reduced using psoralen + UVA light.

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3
Q

What is the purpose of pathogen reduction (e.g., INTERCEPT system)?

A

To inactivate viruses, bacteria, and parasites using amotosalen (psoralen) + UVA light.

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4
Q

What are the storage conditions for platelets?

A

20–24°C with continuous agitation; shelf life = 7 days.

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5
Q

Why is agitation of platelets necessary?

A

Facilitates gas exchange and prevents aggregation.

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6
Q

When is irradiation required for platelets?

A

For immunocompromised patients or HLA-matched/related donors to prevent GVHD.

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7
Q

When are platelet transfusions indicated?

A

For bleeding/thrombocytopenia (e.g., post-chemo, surgery) or prophylactically for very low counts.

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8
Q

What are contraindications for platelet transfusion?

A

ITP/TTP/HIT (unless life-threatening bleeding) (because all platelets are getting destroyed regardless)
Hypersensitivity to psoralen (for pathogen-reduced platelets).

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9
Q

Why is HLA matching important for platelets?

A

Platelets express Class I HLA (A, B, C). HLA antibodies (from pregnancy/transfusion) can destroy unmatched platelets, causing refractoriness.

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10
Q

How is platelet refractoriness managed?

A

Use HLA-matched or HPA-matched (for anti-HPA antibodies) apheresis platelets.

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11
Q

What causes TRALI?

A

Donor HLA antibodies (often from multiparous females) activating recipient neutrophils.

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12
Q

What is Post-Transfusion Purpura (PTP)?

A

Severe thrombocytopenia 7–14 days post-transfusion due to anti-HPA-1a (most common).

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13
Q

What is FNAIT?

A

Fetal thrombocytopenia from maternal anti-HPA antibodies crossing the placenta.

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14
Q

what are the risks of ABO-incompatible platelets?

A

Passive anti-A/B in donor plasma can cause hemolysis (e.g., Group O platelets to Group A patient).

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15
Q

Volume of pooled platelets?

A

~184 mL (vs. ~317 mL for older methods).

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16
Q

Leukocyte limits in platelet products?

A

<5 × 10⁶ (apheresis) or <10 × 10⁶ (pooled).

17
Q

Residual infection risks (per donation) of platelet products?

A

HIV: 1 in 21.4 million
HCV: 1 in 12.6 million

18
Q

A Group A patient gets a positive DAT after O platelets. Cause?

A

Anti-A/B from donor plasma coating recipient RBCs.

19
Q

What is the priority for platelet selection?

A

ABO identical > compatible > alternative

20
Q

How is HLA typing performed?

A

Microlymphocytotoxicity (CDC) or flow cytometry.

21
Q

Which cells are involved in HLA Class I vs. II?

A

Class I: All nucleated cells (A, B, C).
Class II: Immune cells (DR, DQ, DP).

22
Q

Why are platelets the most associated with bacterial sepsis?

A

Because the platelets are pooled

23
Q

Which class of HLAs are on the surface of platelets, leukocytes, and retics?

24
Q

Which class of HLAs are on immunocompetent cells such as B lymps, activated T lymphs, macrophages, and endothelial cells?

25
What is refractoriness?
When a patient is unresponsive to platelet transfusions
26
What can cause platelet refractoriness?
HLA-specific or platelet-specific antibodies and/or platelet destruction from fever or sepsis
27
What 3 conditions are immune causes of platelet refractoriness?
HLA alloantibodies Platelet alloantibodies Autoantibodies
28
What 6 conditions are non-immune causes of platelet refractoriness?
Splenomegaly Medications Sepsis Active bleeding DIC Fever