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G. N. Callahan

Researcher at Colorado State University

Publications -  39
Citations -  1857

G. N. Callahan is an academic researcher from Colorado State University. The author has contributed to research in topics: Antigen & Major histocompatibility complex. The author has an hindex of 16, co-authored 39 publications receiving 1852 citations. Previous affiliations of G. N. Callahan include University of Florida & Scripps Health.

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On the thymus in the differentiation of "H-2 self-recognition" by T cells: evidence for dual recognition?

TL;DR: Adult thymectomized, irradiated and bone marrow reconstituted mice, transplanted with an irradiated thymus of A origin, generate virus-specific cytotoxic T cells specific for infected A targets but not for B targets; this result formally demonstrates the crucial role of thymic epithelial cells in the differentiation of anti-self-H-2 specificities of T cells.
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The lymphoreticular system in triggering virus plus self-specific cytotoxic T cells: evidence for T help.

TL;DR: If T cells learn in the thymus to recognize H-21 or K, D markers that are not at least partially carried themselves in other cells of the lymphoreticular system immunological interactions will be impossible and this paradox situation results in phenotypic immune incompetence in vivo.
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Restriction specificities, alloreactivity, and allotolerance expressed by T cells from nude mice reconstituted with H-2-compatible or -incompatible thymus grafts.

TL;DR: The discrepancy between the restorative capacity of unirradiated vs. irradiated thymus grafts suggests that precursors of T cells in nude mice can acquire restriction specificity and immunocompetence independently of a conventional, functioning H-2-compatibleThymus if exposed to an allogeneic fetal or a newborn thymu that contains functioning thymocytes of donor type but not if reconstituted with an irradiated adult allogeneIC thymUS.
Journal Article

Biologic and Chemical Characterization of HLA Antigens in Human Serum

TL;DR: The purified lipid-associated antigen was immunogenic since it elicited the formation of cytotoxic xenoantibodies in rabbits and suggests that HLA antigens are shed into plasma as a complex of a single HLA molecule and a single beta2-microglobulin chain, associated with boundary lipid.