Analysis of the immunological mechanisms in the F1 hybrid anti-parental reactivity, and detection of a new minor histocompatibility 42(H-42) locus by F1 cytotoxic T lymphocytes generated under the condition of graft-versus-host reaction.
スポンサーリンク
概要
- 論文の詳細を見る
Lethally X-irradiated F1 hybrid mice of some strains do not accept bone marrow transplants from one or another of the parental strains, and normal unirradiated F1 mice often exert resistance against the graft-vs-host reaction (GvHR)-associated immunosuppression induced by lymphocytes from a certain parental strain. Moreover, normal F1 mouse spleen cells can respond to parental antigen coded for by the major histocompatibility complex (MHC) and generate cytotoxic T lymphocytes, which specifically kill target cells bearing the homozygous parental MHC antigens, in primary in vitro cultures. All of these phenomena are apparently a violation of the basic law of classical transplantation immunity in which the co-dominant phenotypic expression of histocompatibility gene products in F1 hybrid animals has been established. Therefore, the study on the mechanisms of these phenomena, called hybrid resistance (HyR), embraces many important yet unexplained aspects of transplantation immunity, and offers current immunology an intriguing issue to be explored.To explore complex genetic events that lead to HyR at cellular level, we have studied in detail the in vitro primary F1 anti-parental cytotoxic responses as well as the F1 resistance against parental lymphocyte-induced GvHR by using various kinds of inbred mouse strains carrying well-characterized genetic background. The regulation of both types of the HyR was found to be controlled in appearance by genes located either in the MHC or non-MHC regions. However, our careful experiments have demonstrated that, in most cases, neither the MHC haplotype alone nor the non-MHC background alone can foretell whether a certain F1 mouse strain exerts the HyR or not. In a certain F1 mouse strain, it has been demonstrated that conspicuous combined action of the MHC and non-MHC genes determines the HyR. Implications of this key observation with respect to the immunologic significance of the HyR, together with the discovery of a new mouse minor H-42 histocompatibility locus, are described in detail in the present review article.
- The Keio Journal of Medicineの論文
著者
-
Ishikawa Hiromichi
Department Of Internal Medicine School Of Medicine Keio University
-
ISHIKAWA HIROMICHI
Department of Microbiology, School of Medicine, Keio University
関連論文
- Pivotal role of CCL25 (TECK)-CCR9 in the formation of gut cryptopatches and consequent appearance of intestinal intraepithelial T lymphocytes
- c-Fos suppresses systemic inflammatory response to endotoxin
- Antigen Feeding Increases Frequency and Antigen-specific Proliferation Ability of Intraepithelial CD4^+ T Cells in αβ T Cell Receptor Transgenic Mice(Food & Nutrition Science)
- Analysis of Cytokine Producing Activity of Intestinal Intraepithelial T Cells from TCR β-Chain and δ-Chain Mutant Mice
- Preface
- Onset of hepatic erythropoiesis after malarial infection in mice
- Usefulness of laparoscopy to find the distal vas deferens during vasovasostomy for a patient with iatrogenic injury of the vas deferens during inguinal herniorrhaphy
- Cadmium nephrotoxicity and evacuation from the body in a rat modeled subchronic intoxication
- Cadmium-induced testicular damage in a rat model of subchronic intoxication
- Body mass index for chronic hemodialysis patients : Stable hemodialysis and mortality
- Surgical treatment for an idiopathic renal arteriovenous fistula with a large aneurysm
- Clinical Experience of Laparoscopic Varicocelectomy in 124 Cases
- DEVELOPMENT AND PHYSIOLOGICAL SIGNIFICANCE OF T CELLS EXPRESSING γδ T CELL ANTIGEN RECEPTORS
- Analysis of the immunological mechanisms in the F1 hybrid anti-parental reactivity, and detection of a new minor histocompatibility 42(H-42) locus by F1 cytotoxic T lymphocytes generated under the condition of graft-versus-host reaction.