Literature DB >> 47893

Genetic control of immune response. The dose of antigen given in aqueous solution is critical in determining which mouse strain is high responder to poly(LTyr, LGlu)-poly(LPro)--poly(LLys).

S Jormalainen, E Mozes, M Sela.   

Abstract

Antibody response to different doses of (T,G)-Pro--L, given in aqueous solution, was investigated in the high responder SJL and low responder DBA/1 strains by measuring hemolytic plaque-forming cells (PFC) in the spleens as well as hemagglutination titers in the sera. The gene responsible for the difference between the two strains in the response to this antigen, given in complete Freund's adjuvant, has been previously denoted Ir-3. This gene is not linked to the major histocompatibility locus. In the response to the optimal dose (1 mug) of antigen, no difference could be shown between the strains. The peak of the response and the numbers of direct and indirect PFC were similar in both strains in the primary and secondary response. After injection of higher doses (10-100 mug) of antigen, both the direct and indirect PFC responses were lower in the low responder than in the high responder strain. Moreover, the peak of the response occurred earlier in the high responder strain in the primary response to the 10 mu dose of antigen. After administration of a suboptimal dose (0.02 mug) of antigen, the low responder strain produced in the primary response 4-20 times more indirect plaques than the high responder strain. Also the number of direct plaques was higher in the low responder than in the high responder strain. The serum antibody responses to the optimal and higher doses of antigen were parallel to the PFC responses. From inhibition of PFC with free antigen, it was concluded that a similar proportion of cells was producing high and low affinity antibodies to (T,G)-Pro--L in both strains. High and low zone tolerance could be induced in the two strains with (T,G)-Pro--L, but no difference could be shown between the strains. It is suggested that the Ir-3 gene plays a role in the regulation of the balance stimulation and suppression according to the dose of antigen given.

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Year:  1975        PMID: 47893      PMCID: PMC2189793          DOI: 10.1084/jem.141.5.1057

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  42 in total

Review 1.  Genetic control of specific immune responses.

Authors:  H O McDevitt; B Benacerraf
Journal:  Adv Immunol       Date:  1969       Impact factor: 3.543

2.  Role of optical configuration in the immunogenicity and specificity of synthetic antigens derived from multichain polyproline.

Authors:  J C Jaton; M Sela
Journal:  J Biol Chem       Date:  1968-11-10       Impact factor: 5.157

3.  Relationship between histocompatibility (H-2) genotype and immune responsiveness to low doses of ovalbumin in the mouse.

Authors:  N M Vaz; E M Vaz; B B Levine
Journal:  J Immunol       Date:  1970-06       Impact factor: 5.422

4.  Genetic control of the antibody response: relationship between immune response and histocompatibility (H-2) type.

Authors:  H O McDevitt; A Chinitz
Journal:  Science       Date:  1969-03-14       Impact factor: 47.728

5.  Genetic control of the immune response of guinea pigs to limiting doses of bovine serum albumin: relationship to the poly-L-lysine gene.

Authors:  I Green; J K Inman; B Benacerraf
Journal:  Proc Natl Acad Sci U S A       Date:  1970-08       Impact factor: 11.205

Review 6.  Analogies between lymphocyte receptors and the resulting humoral antibodies.

Authors:  O Mäkelä
Journal:  Transplant Rev       Date:  1970

7.  Infectious immunological tolerance.

Authors:  R K Gershon; K Kondo
Journal:  Immunology       Date:  1971-12       Impact factor: 7.397

8.  Influence of genetic factors on the magnitude and the heterogeneity of the immune response in the rabbit.

Authors:  K Eichmann; D G Braun; R M Krause
Journal:  J Exp Med       Date:  1971-07-01       Impact factor: 14.307

9.  Genetic control of the antibody response in inbred mice. Transfer of response by spleen cells and linkage to the major histocompatibility (H-2) locus.

Authors:  H O McDevitt; M L Tyan
Journal:  J Exp Med       Date:  1968-07-01       Impact factor: 14.307

10.  Contribution of bone marrow cells and lack of expression of thymocytes in genetic controls of immune responses for two immunopotent regions within poly-(Phe,Glu)-poly-Pro--poly-Lys in inbred mouse strains.

Authors:  E Mozes; G M Shearer
Journal:  J Exp Med       Date:  1971-07-01       Impact factor: 14.307

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  4 in total

1.  Immune response inversion after hyperimmunisation. Possible mechanism in the pathogenesis of HLA-linked diseases.

Authors:  C R Young; A Ebringer; J R Archer
Journal:  Ann Rheum Dis       Date:  1978-04       Impact factor: 19.103

2.  Polygenic control of the immune response to F antigen.

Authors:  D M Silver; D P Lane
Journal:  Immunogenetics       Date:  1981       Impact factor: 2.846

3.  Enhancement of certain biological activities of muramyl dipeptide derivatives after conjugation to a multi-poly(DL-alanine)--poly(L-lysine) carrier.

Authors:  L Chedid; M Parant; F Parant; F Audibert; F Lefrancier; J Choay; M Sela
Journal:  Proc Natl Acad Sci U S A       Date:  1979-12       Impact factor: 11.205

4.  Colony-stimulating activity induced by synthetic muramyl peptides: variation with chemical structure and association with anti-infectious activity.

Authors:  A Galelli; P Lefrancier; L Chedid
Journal:  Infect Immun       Date:  1984-11       Impact factor: 3.441

  4 in total

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