Literature DB >> 3089348

The structure of the T cell antigen receptor genes in normal and malignant T cells.

M D Minden, T W Mak.   

Abstract

In this review the genomic structure and the RNA transcripts of the alpha and beta chain of the T cell antigen receptor have been discussed. Studies of the structure of TcR beta in hematologic malignancies have revealed rearrangement in almost all of the T cell malignancies and a small proportion of non-T cell malignancies. In addition, clonal involvement of T cells in diseases such as Hodgkin's disease, angioimmunoblastic lymphadenopathy, and chronic T cell lymphocytosis have been observed. The study of the structure of the TcR beta gene is thus a useful tool for identifying clonal expansions of cells and in conjunction with studies of the immunoglobulin gene structure, and cell surface markers a useful tool for identifying cell lineage. At the present time the evaluation of the structure of the alpha chain genes has not been as fruitful. However, chromosome translocations involving the TcR alpha chain genes have been recognized and, in one case, this rearrangement has been in association with a known oncogene. With the isolation of more probes to the alpha chain region it should be possible to test its utility in identifying clonal populations and cell lineage. The recent isolation of the gamma gene of the T cell will also permit such studies. Preliminary results of studies carried out with a probe to the gamma chain gene of the T cell have paralleled results obtained with the TcR beta probe (unpublished observation).

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Year:  1986        PMID: 3089348

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  21 in total

1.  Rearrangement of the genes for the beta and gamma chains of the T cell receptor is rarely observed in adult B cell lymphoma and chronic lymphocytic leukemia.

Authors:  A C Aisenberg; B M Wilkes; J O Jacobson
Journal:  J Clin Invest       Date:  1987-10       Impact factor: 14.808

2.  Lymphomas of true histiocytic origin. Expression of different phenotypes in so-called true histiocytic lymphoma and malignant histiocytosis.

Authors:  S M Hsu; Y S Ho; P L Hsu
Journal:  Am J Pathol       Date:  1991-06       Impact factor: 4.307

Review 3.  Ontogeny of the human thymus during fetal development.

Authors:  D F Lobach; B F Haynes
Journal:  J Clin Immunol       Date:  1987-03       Impact factor: 8.317

4.  Cultured Reed-Sternberg cells HDLM-1 and KM-H2 can be induced to become histiocytelike cells. H-RS cells are not derived from lymphocytes.

Authors:  S M Hsu; S S Xie; P L Hsu
Journal:  Am J Pathol       Date:  1990-08       Impact factor: 4.307

5.  Molecular cloning of the translocation breakpoint in T-ALL 11;14 (p13;q11): genomic map of TCR alpha and delta region on chromosome 14q11 and long-range map of region 11p13.

Authors:  B Royer-Pokora; B Fleischer; S Ragg; U Loos; D Williams
Journal:  Hum Genet       Date:  1989-06       Impact factor: 4.132

6.  Mammalian T-lymphocyte antigen receptor genes: genetic and nongenetic potential to generate variability.

Authors:  J T Epplen; J Chluba; C Hardt; A Hinkkanen; V Steimle; H Stockinger
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132

Review 7.  Gene-modified cells for stem cell transplantation and cancer therapy.

Authors:  Malcolm K Brenner
Journal:  Hum Gene Ther       Date:  2014-07       Impact factor: 5.695

8.  Proposals for the classification of chronic (mature) B and T lymphoid leukaemias. French-American-British (FAB) Cooperative Group.

Authors:  J M Bennett; D Catovsky; M T Daniel; G Flandrin; D A Galton; H R Gralnick; C Sultan
Journal:  J Clin Pathol       Date:  1989-06       Impact factor: 3.411

9.  Quantitation of mu mRNA by in situ hybridization reveals a correlation between B-maturation associated antigens and IgM gene activation in acute lymphatic leukemias.

Authors:  K Pachmann; B Dörken; B Emmerich; E Thiel
Journal:  Med Oncol Tumor Pharmacother       Date:  1988

10.  T lymphocytes in giant cell arteritic lesions are polyclonal cells expressing alpha beta type antigen receptors and VLA-1 integrin receptors.

Authors:  C Schaufelberger; S Stemme; R Andersson; G K Hansson
Journal:  Clin Exp Immunol       Date:  1993-03       Impact factor: 4.330

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