Literature DB >> 5682942

Quantitative studies on the mixed lymphocyte interaction in rats. 3. Kinetics of the response.

D B Wilson, P C Blyth JL NOWELL.   

Abstract

The proliferative interaction of cultured rat lymphocytes of immunogenetically disparate origin-the mixed lymphocyte interaction-was employed as an experimental model to examine the initial stages of the immune response mechanism. Using mixed cultures of cells derived from parental strain and F(1) hybrid rats, in which only the parental lymphocytes respond, the following observations were made on the magnitude and kinetics of the reaction. After initiation of the cultures, there was a latent period of approximately 40 hours during which time no mitotic activity was detected. This inactive phase was followed by a period of proliferation in which previously nondividing cells entered the mitotic cycle for the first time. Activity in the cultures, as detected by incorporation of radioactive thymidine and measured by radioautography or scintillation spectrometry, increased exponentially with a doubling time (T2) of 9-10 hr. In this exponential proliferative phase, lasting approximately 100 hr, the dividing cells underwent a series of rapid sequential divisions with a generation time (Tc) of 8 hr, and few, if any, dropped out of the mitotic cycle. In addition to the cells which first entered mitosis at the beginning of the proliferative phase and then proceeded through multiple divisions, significant numbers of new, previously nondividing cells continued to enter the mitotic cycle during the entire exponential growth phase. The total number of these newly responsive, first division cells throughout the total culture period amounted to 1-3% of the original parental cell inoculum. This is a surprisingly large proportion of peripheral blood lymphocytes with demonstrable reactivity to a particular antigen system, if it is assumed that these first division cells in vitro are functionally related to the hypothetical antigen-sensitive cells which proliferate and differentiate into immunological effector cells. At present there is no entirely satisfactory explanation for this large number of reactive cells in the mixed lymphocyte interaction.

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Year:  1968        PMID: 5682942      PMCID: PMC2138568          DOI: 10.1084/jem.128.5.1157

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


  22 in total

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Authors:  B BAIN; M R VAS; L LOWENSTEIN
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2.  RADIOSENSITIVITY OF THE IMMUNE RESPONSE TO SHEEP RED CELLS IN THE MOUSE, AS MEASURED BY THE HEMOLYTIC PLAQUE METHOD.

Authors:  J C KENNEDY; J E TILL; L SIMINOVITCH; E A MCCULLOCH
Journal:  J Immunol       Date:  1965-05       Impact factor: 5.422

3.  Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors:  P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
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4.  The immunologic significance of antigen induced lymphocyte transformation in vitro.

Authors:  J A Mills
Journal:  J Immunol       Date:  1966-08       Impact factor: 5.422

5.  Further studies of histocompatibility loci in rats.

Authors:  H Ramseier; J Palm
Journal:  Transplantation       Date:  1967-07       Impact factor: 4.939

6.  Mixed leukocyte reactions and histocompatibility in rats.

Authors:  W K Silvers; D B Wilson; J Palm
Journal:  Science       Date:  1967-02-10       Impact factor: 47.728

7.  A method for counting phytohemagglutinin-stimulated lymphocytes.

Authors:  C C Stewart; M Ingram
Journal:  Blood       Date:  1967-04       Impact factor: 22.113

8.  Growth and senescence of antibody-forming cells.

Authors:  J F Albright; T Makinodan
Journal:  J Cell Physiol       Date:  1966-06       Impact factor: 6.384

9.  Chorioallantoic membrane lesions produced by inoculation of adult fowl small lymphocytes.

Authors:  M J Simons; R Fowler
Journal:  Nature       Date:  1966-02-05       Impact factor: 49.962

10.  Quantitative studies on the mixed lymphocyte interaction in rats. I. Conditions and parameters of response.

Authors:  D B Wilson
Journal:  J Exp Med       Date:  1967-10-01       Impact factor: 14.307

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  79 in total

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2.  The receptor specificity of alloreactive T cells. Distinction between stimulator K, I, and D region products and degeneracy of third-party H-2 recognition by low-affinity T cells.

Authors:  Z A Nagy; B E Elliott
Journal:  J Exp Med       Date:  1979-12-01       Impact factor: 14.307

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Review 4.  Alloimmune T cells in transplantation.

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5.  Antigen-binding small lymphocytes in the guinea-pig. II. The immunological response to purified protein derivative of mammalian tuberculin.

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6.  Reconstitution of immunocompetence in B cells by addition of concanavalin A or concanavalin A-treated thymus cells.

Authors:  O Sjöberg; G Möller; J Andersson
Journal:  Clin Exp Immunol       Date:  1973-02       Impact factor: 4.330

7.  Quantitative studies on the proliferation and differentiation of antibody-forming cells in lymph.

Authors:  J B Hay; M J Murphy; B Morris; M C Bessis
Journal:  Am J Pathol       Date:  1972-01       Impact factor: 4.307

8.  Quantitative studies on the mixed lymphocyte interaction in rats. V. Tempo and specificity of the proliferative response and the number of reactive cells from immunized donors.

Authors:  D B Wilson; P C Nowell
Journal:  J Exp Med       Date:  1971-03-01       Impact factor: 14.307

9.  Human T cells expressing V beta 8 do not predominantly recognize DR2 alloantigen.

Authors:  S E Christmas; R Brew; I Crosby; I E Gecim; R A Sells
Journal:  Immunology       Date:  1992-06       Impact factor: 7.397

10.  Activation of leukemia viruses by graft-versus-host and mixed lymphocyte reactions in vitro.

Authors:  M S Hirsch; S M Phillips; C Solnik; P H Black; R S Schwartz; C B Carpenter
Journal:  Proc Natl Acad Sci U S A       Date:  1972-05       Impact factor: 11.205

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