Literature DB >> 2426352

Activation requirements of cloned inducer T cells. III. Need for two stimulator cells in the response of a cloned line to Mls determinants.

R H DeKruyff, S T Ju, J Laning, H Cantor, M E Dorf.   

Abstract

To gain insight into the nature of Mls determinants, we examined the stimulator cells responsible for the activation of inducer T cell clones by Mls determinants. Two types of clones responding to Mls determinants were identified. One type responded to purified B cells, but not to splenic adherent cells (SAC), from mice bearing Mls stimulatory determinants. The other type of Mls-reactive T cell clone, including the representative clone Ly1-N5, demonstrated a vigorous response to unfractionated spleen cells, but showed little or no response to B cells alone or to SAC alone from mice bearing the Mlsa or Mlsd stimulatory determinant. The response of these clones to Mls determinants required stimulation by two cell types. The failure of clone Ly1-N5 to respond to Mlsa-bearing B cells was reversed by the addition of SAC taken from mice bearing the Mlsa allele. In addition, SAC from mice bearing the nonstimulatory Mlsb allele could synergize with B cells from Mlsa-bearing animals. B cells were required to provide the Mlsa determinant, because the combination of Mlsa-bearing SAC and Mlsb-bearing B cells did not activate the clone. The response of clone Ly1-N5 to Mls is restricted by Ia determinants (shared by H-2b, H-2d, and H-2k haplotypes but not by the H-2q haplotype). The permissive H-2 alleles can be present either on the stimulator B cell or on the SAC. The optimal response of the clone was obtained by using B cells bearing Mlsa and the permissive Ia epitopes. However, a significant response of the clone to B cells bearing Mlsa but an inappropriate Ia (Iaq) was also seen in the presence of SAC bearing the nonstimulatory Mlsb allele but the permissive Ia epitopes.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 2426352

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  10 in total

1.  A highly sensitive in vitro infection assay to explore early stages of mouse mammary tumor virus infection.

Authors:  S Vacheron; T Renno; H Acha-Orbea
Journal:  J Virol       Date:  1997-10       Impact factor: 5.103

Review 2.  Role of the T cell receptor alpha-chain in superantigen recognition.

Authors:  M A Blackman; D L Woodland
Journal:  Immunol Res       Date:  1996       Impact factor: 2.829

3.  The J alpha segment contributes to the affinity of V beta 6+ cells for vSAG-7 (Mls-1a) presented by I-A molecules.

Authors:  E Churaqui; M Oukka; F Tilloy; E Mayadoux; M Bruley-Rosset; K Kosmatopoulos
Journal:  Immunology       Date:  1995-04       Impact factor: 7.397

4.  CD8+ T cells respond clonally to Mls-1a-encoded determinants.

Authors:  H R MacDonald; R K Lees; Y Chvatchko
Journal:  J Exp Med       Date:  1990-04-01       Impact factor: 14.307

5.  T cell receptor-major histocompatibility complex class II interaction is required for the T cell response to bacterial superantigens.

Authors:  N Labrecque; J Thibodeau; W Mourad; R P Sékaly
Journal:  J Exp Med       Date:  1994-11-01       Impact factor: 14.307

6.  Major histocompatibility complex-specific recognition of Mls-1 is mediated by multiple elements of the T cell receptor.

Authors:  D L Woodland; H P Smith; S Surman; P Le; R Wen; M A Blackman
Journal:  J Exp Med       Date:  1993-02-01       Impact factor: 14.307

7.  Paracrine transfer of mouse mammary tumor virus superantigen.

Authors:  M Delcourt; J Thibodeau; F Denis; R P Sekaly
Journal:  J Exp Med       Date:  1997-02-03       Impact factor: 14.307

8.  Analysis of Mlsc genetics. A novel instance of genetic redundancy.

Authors:  R Abe; M Foo-Phillips; R J Hodes
Journal:  J Exp Med       Date:  1989-10-01       Impact factor: 14.307

9.  Clonal deletion of self-reactive T cells in irradiation bone marrow chimeras and neonatally tolerant mice. Evidence for intercellular transfer of Mlsa.

Authors:  D E Speiser; R Schneider; H Hengartner; H R MacDonald; R M Zinkernagel
Journal:  J Exp Med       Date:  1989-08-01       Impact factor: 14.307

10.  Human T cells respond to mouse mammary tumor virus-encoded superantigen: V beta restriction and conserved evolutionary features.

Authors:  N Labrecque; H McGrath; M Subramanyam; B T Huber; R P Sékaly
Journal:  J Exp Med       Date:  1993-06-01       Impact factor: 14.307

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.