In vitro preacdvated human T cells engraft in SCID mice and migrate to murine lymphoid tissues

Author:

ARMSTRONG N1,CIGEL F1,BORCHERDING W2,HONG R2,MALKOVSKA V1

Affiliation:

1. Department of Medicine, University of Wisconsin, Madison, WI, USA

2. Department of Immunology, University of Wisconsin, Madison, WI, USA

Abstract

SUMMARY Mice with severe combined immunodeficiency (SCID) accept grafts of human T and B lymphocytes derived from resting peripheral blood mononuclear cells (PBMC). We wished to determine whether activated human T cells engraft and migrate into lymphoid tissues in SCID mice. PBMC (50 × 106) activated in vitro in a 4-day mixed lymphocyte culture (MLC) were injected into the peritoneum of 12 SCID mice. In 11 of 12 animals killed at 3 or 4 weeks after injection, human cells were detected in cells pooled from lymphoid organs by flow cylomctry and by immunohistochemical staining of frozen tissue sections. The percentage of CD45+ cells in the 11 mice ranged from 2% to 45% and the absolute numbers of CD45+ cells recovered from lymphoid organs ranged from 4 × 106 to 90 × 106. Up to 93% of the human cells expressed the CD3 antigen together with either CD4 or CDS. Human T cells were localized in periarteriolar areas in murine spleens, whereas in the lymph nodes and gut mucosa, the T cells did not show the pattern for T-dependcnt areas found in human lymphoid tissue. Numerous human plasma cells were detected in the spleen and gut mucosal crypts of engrafted SCID mice. Human IgG was delected in the serum of all 11 engrafted SCID mice. The functional activity of human T cells recovered from murine splenic tissue was very low 3–4 weeks after engraftment.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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