Abstract |
In previous studies it was found that BALB/c (H-2d) was more susceptible than (BALB/c X A)F1 (H-2d X H-2a) to a tumor bearing multiple mismatched minor histocompatibility antigens, the DBA/2 (H-2d) mastocytoma P815, and that this resistance was H-2 linked. In the present studies the immunologic basis of this effect was examined by comparing the cytotoxic-T-lymphocyte (CTL) responses of BALB/c with those of (BALB/c X A)F1. Despite the BALB/c X A)F1's 34-fold greater resistance to P815 in vivo, the numbers of effector cell precursors were found to be similar in the two hosts as shown by (a) similar anti-P815 CTL responses in vitro with T-cell growth factor, (b) similar secondary anti-DBA/2 MiHA responses after in vivo priming with irradiated P815, and (c) similar frequencies of anti-DBA/2 CTL precursors by limiting-dilution analysis. However, priming with proliferating P815 in vivo revealed a defect in the BALB/c animals: Spleen cells from such animals were unable to control the growth of contaminating P815 cells in vitro or to mount strong secondary CTL responses to DBA/2 antigens. The defective priming of BALB/c could be corrected when DBA/2 spleen cells were added to the P815 inoculum. This impaired priming by living tumor cells was not seen in (BALB/c X A)F1. It is concluded that the use of living P815 tumor cells revealed a defect in immunoregulation in BALB/c mice, which rendered them susceptible to tumor growth in spite of apparently adequate numbers of anti-minor-CTL precursors. How the additional H-2 products expressed in the (BALB/c X A)F1 might correct this defect is discussed.
|
Authors | G Carayanniotis, P F Halloran |
Journal | Cellular immunology
(Cell Immunol)
Vol. 91
Issue 1
Pg. 100-10
(Mar 1985)
ISSN: 0008-8749 [Print] Netherlands |
PMID | 2857596
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Antigens, Neoplasm
- Interleukin-2
|
Topics |
- Animals
- Antigens, Neoplasm
(administration & dosage, immunology)
- Cytotoxicity Tests, Immunologic
- Female
- Immunity, Innate
- Immunization, Secondary
- Interleukin-2
(physiology)
- Lymphocyte Transfusion
- Lymphocytes
(radiation effects)
- Lymphoma
(genetics, immunology)
- Mast-Cell Sarcoma
(genetics, immunology)
- Mice
- Mice, Inbred BALB C
- Mice, Inbred C57BL
- Mice, Inbred DBA
- Minor Histocompatibility Loci
- Neoplasm Transplantation
- Rats
- Rats, Inbred Lew
- Stem Cells
(immunology)
- T-Lymphocytes
(immunology)
- T-Lymphocytes, Cytotoxic
(immunology)
|