SearchDictionaryMobileLogin

Prevention of granuloma development in the mouse by using T cell hybridoma products.

AbstractThe ability of an azobenzenearsonate (ABA)-specific suppressor T cell factor, a soluble extract from first order suppressor T cells (Ts1), and suppressor molecules produced by a long-term T cell hybridoma to regulate ABA-specific granuloma formation was studied. ABA-derivatized syngeneic spleen cells (ABA-SC) administered subcutaneously induced persistent delayed-type hypersensitivity (DTH) responses, detected by footpad swelling and hapten-specific granuloma formation by 72 and 96 hr after challenge with ABA-bovine serum albumin coupled to polyacrylamide beads (ABA-BSA-PAB). Soluble factors from ABA-specific Ts1 prevented DTH and granulomatous development after subcutaneous administration of ABA-SC. Moreover, the in vivo administration of a factor that is derived from a Ts1 functioning hybrid cell line induced a second set of suppressor cells (Ts2) that upon transfer to syngeneic ABA-primed mice were able to inhibit granuloma formation in the footpad, as well as in the gastrointestinal tract after challenge with ABA-BSA-PAB. These experiments demonstrate the dependence of the granulomatous reaction on T cell-mediated events, as well as the potential therapeutic efficacy of an antigen-specific suppressor T cell factor and a hybridoma T cell product in limiting antigen-specific granuloma formation in vivo.
AuthorsC H Ginsburg, J T Dambrauskas, R B Whitaker, Z M Falchuk, M I Greene
JournalJournal of immunology (Baltimore, Md. : 1950) (J Immunol) Vol. 132 Issue 1 Pg. 203-8 (Jan 1984) ISSN: 0022-1767 UNITED STATES
PMID6197444 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Epitopes
  • Lymphokines
  • Suppressor Factors, Immunologic
  • p-Azobenzenearsonate
Topics
  • Animals
  • Disease Models, Animal
  • Epitopes
  • Female
  • Granuloma (immunology, pathology, therapy)
  • Hybridomas (immunology, metabolism)
  • Hypersensitivity, Delayed (immunology, therapy)
  • Lymphokines (administration & dosage)
  • Mice
  • Mice, Inbred A
  • Suppressor Factors, Immunologic
  • T-Lymphocytes, Regulatory (immunology, metabolism)
  • p-Azobenzenearsonate (immunology)