Exam 17: The Immune Response

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Which cells of the immune system produce IFN-ɤ and protect the body against intracellular pathogens by activating macrophages to kill pathogens they might harbor?

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Chimeric antigen receptors (CARs)have evolved in molecular structure through three generations of design. Which of the following statements regarding the three generations of CARs is correct?

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Which of the antigens below are typically able to activate B cells without the involvement of T cells?

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Antigens that originate within the cytosol of a cell are referred to as __________.

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What is found on the surface of T cells?

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Which of the following are proteolytic enzymes that enter perforin channels and activate caspases, which in turn initiate the apoptotic response?

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Who realized that a cowpox infection at an early age protected people against deadly smallpox infections?

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Some activated B cells differentiate into short-lived cells that secrete large amounts of antibodies. Such cells are called __________.

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What fatal disease is characterized by severe autoimmunity in newborn infants and is caused by a mutation in a gene that encodes a transcription factor required for the differentiation of TReg cells?

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B cells are activated by ________ and T cells are activated by ______.

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What is the source of activated B cell populations?

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Which antibodies are the predominant antibodies found in blood and lymph during a secondary response to most antigens?

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What is usually required for B cell activation by an antigen?

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Which of the following is characteristic of immature T cells that have just migrated to the thymus gland from the bone marrow?

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The human genome has been shown to code for 51 different functional VH segments, 25 different DH segments and 6 JH segments for the heavy chain variable regions of antibodies. Assuming that any V segment can combine with any of the D and J segments, how many different heavy chains could be made?

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Why are the second and subsequent responses to antigen exposure faster than the initial response?

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Blood contains a group of soluble proteins, which bind extracellular pathogens and destroy them. In one case, an assembly of these activated soluble proteins perforates the bacterial cell membrane, causing lysis and death of the cells. What is this group of soluble proteins called?

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Which antibodies have no clearly understood function?

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Which is NOT a present-day challenge in the clinical use of adoptive T cell therapy?

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In what way does the character of the antibodies made during a secondary response differ from those made during the primary response?

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