Low IgG response of the mouse strain C57BL/10ScSn after immunization with protein antigens
Language English Country United States Media print
Document type Journal Article
PubMed
4007712
DOI
10.1007/bf02923523
Knihovny.cz E-resources
- MeSH
- Antigens MeSH
- Arsenates immunology MeSH
- Immunization MeSH
- Immunoglobulin G biosynthesis MeSH
- Immunoglobulin M biosynthesis MeSH
- Immunologic Memory MeSH
- Mice, Inbred A immunology MeSH
- Mice, Inbred C57BL immunology MeSH
- Mice MeSH
- Proteins immunology MeSH
- Trinitrobenzenes immunology MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Antigens MeSH
- Arsenates MeSH
- Immunoglobulin G MeSH
- Immunoglobulin M MeSH
- Proteins MeSH
- Trinitrobenzenes MeSH
The low IgG response of the strain C57BL/10ScSn is not restricted to the reaction to sheep red blood cells; but it can be demonstrated even after immunization with ARS, DNP or FITC haptens, coupled to various heterologous (BGG, RSA) or autologous (MGG) protein carriers. The level of the IgG response is - using the same immunization schedule - influenced both by the bound hapten and the carrier. In both strains tested (i.e. in the high-responding A/J and the low-responding C57BL/10ScSn), the highest IgG response is elicited by FITC-BGG. The response of the C57BL/10ScSn strain is, similarly as after immunization with SRBC, approximately ten times lower. The IgG response to other antigens tested was lower in both strains and therefore the quantitative differences were less pronounced. The affinity of antibodies against the ARS and TNP determinant, detected by inhibition of plaque-forming cells, is similar in the two strains. Thus the low reactivity of the strain C57BL/10ScSn is not caused by the absence of suitable VH and VL genes, but it rather indicates a defect of some general regulatory mechanism, involved in the synthesis of IgG antibodies. After repeated administration of ARS-BGG, the antigen and the antigen - antibody complexes accumulate in high concentrations primarily in the liver of mouse strain A/J. The amount of antigen accumulated in the liver of strain C57BL/10ScSn is significantly lower.
See more in PubMed
Folia Biol (Praha). 1981;27(1):1-14 PubMed
Am J Reprod Immunol. 1981 Aug;1(4):164-7 PubMed
J Exp Med. 1975 Mar 1;141(3):647-63 PubMed
J Immunol Methods. 1980;38(3-4):251-6 PubMed
Immunol Lett. 1983;7(3):145-9 PubMed
Eur J Immunol. 1983 Mar;13(3):269-72 PubMed
Proc Soc Exp Biol Med. 1969 Nov;132(2):575-81 PubMed
Folia Biol (Praha). 1984;30(1):57-66 PubMed
Am J Reprod Immunol. 1981 Aug;1(4):168-73 PubMed
J Exp Med. 1972 Nov 1;136(5):1063-71 PubMed