Humans with defective expression of the integrin LFA-1 have an immunodeficiency disease characterized by the failure of lymphocytes and granulocytes to migrate to tissues at sites of infection or inflammation. A similar immunodeficiency would be expected if individuals had mutations disrupting the gene for:
A) CD3
B) The complement receptor, CD21
C) WASp
D) Rap1
E) SLP-76
Correct Answer:
Verified
Q21: A mutant B cell line is
Q22: Unlike TCR signaling, B cell receptor (BCR)
Q23: Antigen receptor signaling and lymphocyte activation.antibody
Q24: T cells with defective TCR signaling
Q25: Phosphorylation of signaling proteins can have activating
Q27: The B cell co-receptor, composed of
Q28: The only mechanism by which CD28 co-stimulation
Q29: TCR and CD28 signaling together lead to
Q30: The integrin LFA-1 is constitutively expressed on
Q31: TCR stimulation was shown to affect ICAM-1
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