Immunodominance in the immune response to “multiple” histocompatibility antigens
✍ Scribed by Peter J. Wettstein; Donald W. Bailey
- Publisher
- Springer-Verlag
- Year
- 1982
- Tongue
- English
- Weight
- 703 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0093-7711
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✦ Synopsis
Cytotoxic effector T cells putatively specific for multiple non-H-2 histocompatibility (H) antigens were generated by immunizing and boosting C57BL/6 and B6.C-H-2 d mice with BALB.B and BALB/c stimulator cells, respectively. The generated effectors were tested for cell-mediated lympholysis on a panel of targets whose BALB/c-derived non-H-2 H antigens were donated by CXB recombinant inbred mice. The spectrum of reactivity of cytotoxic effector T cells with CXB targets demonstrated that the effectors did not recognize multiple H antigens but rather preferentially recognized a single immunodominant non-H-2 H antigen. The identity of the immunodominant H antigen was determined by the H-2 genotype of the stimulator cells when (B6 x B6.C-H-2d)F1 cytotoxic effectors were tested. These observations indicate that despite the fact that responders were challenged with more than 40 individual non-H-2 H antigens, they preferentially responded to a single immunodominant antigen.
📜 SIMILAR VOLUMES
The histocompatibility (H) system comprises a large number of loci responsible for acceptance and rejection of both neoplastic and normal tissue. The H-2 locus is the mouse major histocompatibility complex (MHC). H-2 class I and class II alloantigens exhibit high antigenic strength, while the remain
## Abstract The lymph node cells of CBA (H‐2^k^), but not BALB/c (H‐2^d^) mice, release interferon (IFN)‐γ into the supernatant when immunized with picryl chloride epicutaneously and then exposed to antigen (haptenized cells) __in vitro__ 4 days later. The failure in IFN‐γ production maps to the ma