Literature DB >> 25290298

On getting a T-cell clone and being assured you have one.

F Bach1.   

Abstract

Cellular immunology has for years been plagued by the heterogeneity in function and specificity of antigen recognition present within the populations of lymphocytes available for study. The ability to clone single T cells from those populations is therefore a most useful technology because the progeny in any one clone will be of a single functional subtype and, at the very least, will have the great specificity associated with monoclonality. Cloning is being widely used to push forward our understanding of both the antigens that elicit response and the cells that respond. My purpose here, however, is not to review those very exciting applications but rather to address the sometimes thorny issues of the definition of clonality, how it is achieved, and the circumstances in which 'proof' of clonality is or is not essential to the interpretation of data.
Copyright © 1983. Published by Elsevier B.V.

Year:  1983        PMID: 25290298     DOI: 10.1016/0167-5699(83)90039-7

Source DB:  PubMed          Journal:  Immunol Today        ISSN: 0167-5699


  2 in total

1.  Human allospecific TLCs generated against HLA antigens associated with DR1 through DRw8. II. Population analyses and blocking studies with monoclonal antibodies.

Authors:  S Rosen-Bronson; A H Johnson; R J Hartzman; D D Eckels
Journal:  Immunogenetics       Date:  1986       Impact factor: 2.846

2.  Proliferative and cytotoxic responses of human peripheral blood lymphocytes to autologous malignant effusions. An analysis at the clonal level.

Authors:  T E Roberts; U Shipton; M Moore
Journal:  Cancer Immunol Immunother       Date:  1986       Impact factor: 6.968

  2 in total

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