
John G. answered 09/07/21
B.S. in Molecular Biology and 3 years of research experience
- This is true becuase T-cell-dependent responses give you class switch to the more useful, more tissue-infiltrating IgG class, and they also give you memory and somatic hypermutation.
- Yes. The majorly important one is B7 on pAPCs, which binds to CD28 on T cells.
- This is true because the a components serve as inflammatory mediators, chemoattractants, and also increase microbicidal capacity of phagocytes like macrophages. They also activate mast cells to promote release of inflammatory compounds like histamine.
- This isn't necessarily true, as an immune response isn't activated against every antigen. For example, self antigens will not elicit an immune response. However, if you find a host to which the antigen is foreign, I suppose you could say any antigen can be an immunogen.
- This is just fact. The only exception is immature and mature naive B cells, who have both IgM and IgD.
- They do so by binding TCR:MHCII complexes and holding them together, which tricks the T cell into thinking it's been activated.
- Take papain for an example. The antigen-binding fragment still remains intact and can still bind specific antigen.
- This is true because class switch only affects the constant region--not the antigen-binding region.