Study for the Missouri EFDA Basic Skills Test. Use flashcards and multiple choice questions, each with hints and explanations. Prepare effectively for your certification exam!

Multiple Choice

HIV affects which type of immune cells once it enters the body?

HIV primarily targets CD4-positive T helper cells, which are the immune system’s coordinators. These cells help activate other parts of the immune response, including B cells and cytotoxic T cells, so their loss cripples both antibody production and targeted killing of infected cells. The virus gains entry by attaching to the CD4 receptor and a co-receptor on these cells, then uses its genetic material to replicate, eventually destroying or disabling the T cells. Over time, depletion of these helpers leads to immune deficiency. B-cells aren’t the main targets, though their function can be indirectly affected as helper T cells decline. Macrophages can be infected by HIV as well, but they are not the primary cells the virus destroys. NK cells aren’t the main targets either; they play a different role in innate immunity. The central issue in HIV infection is the loss and dysfunction of CD4+ T helper cells.

HIV primarily targets CD4-positive T helper cells, which are the immune system’s coordinators. These cells help activate other parts of the immune response, including B cells and cytotoxic T cells, so their loss cripples both antibody production and targeted killing of infected cells. The virus gains entry by attaching to the CD4 receptor and a co-receptor on these cells, then uses its genetic material to replicate, eventually destroying or disabling the T cells. Over time, depletion of these helpers leads to immune deficiency.

B-cells aren’t the main targets, though their function can be indirectly affected as helper T cells decline. Macrophages can be infected by HIV as well, but they are not the primary cells the virus destroys. NK cells aren’t the main targets either; they play a different role in innate immunity. The central issue in HIV infection is the loss and dysfunction of CD4+ T helper cells.