Q.12 What is true about MHC class II? 1. Present extracellular peptides to CD8+ cells 2. Present intracellular peptides to CD8+ cells 3. Present extracellular peptides to CD4+ cells 4. Present intracellular peptides to CD4+ cells

Q.12 What is true about MHC class II?

1. Present extracellular peptides to CD8+ cells

2. Present intracellular peptides to CD8+ cells

3. Present extracellular peptides to CD4+ cells

4. Present intracellular peptides to CD4+ cells

MHC class II molecules are key players in the adaptive immune system, primarily presenting extracellular peptides to CD4+ T cells. The correct answer to the multiple-choice question is option 3.

Correct Answer

Option 3: Present extracellular peptides to CD4+ cells.
MHC class II molecules, expressed mainly on antigen-presenting cells like dendritic cells, macrophages, and B cells, load peptides from extracellular pathogens degraded in endosomes/lysosomes. These peptide-MHC II complexes are recognized by CD4+ helper T cells, activating cytokine production and immune coordination.

Option Breakdown

Option Statement Correct/Incorrect Explanation
1 Present extracellular peptides to CD8+ cells Incorrect MHC class II handles extracellular peptides, but CD8+ cytotoxic T cells recognize MHC class I, not class II.
2 Present intracellular peptides to CD8+ cells Incorrect Intracellular peptides (e.g., from viruses) are presented by MHC class I to CD8+ cells; MHC II does not.
3 Present extracellular peptides to CD4+ cells Correct This matches MHC II’s core role: exogenous antigens processed via endocytosis and presented to CD4+ helper T cells for humoral immunity.
4 Present intracellular peptides to CD4+ cells Incorrect MHC II primarily presents extracellular peptides; intracellular ones go to MHC I/CD8+ pathway (minor autophagy exceptions exist but not primary).

MHC Class II Pathway

Antigens from extracellular sources (bacteria, toxins) are engulfed by APCs, degraded in lysosomes, and bind MHC II in a specialized compartment. The complex moves to the surface for CD4+ T cell activation, driving B cell help and macrophage activation. This contrasts with MHC I, which uses cytosolic proteasomes for endogenous antigens.

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