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PMID: 1691221 Published · ppublish English Journal Article

Targeted cytotoxic cells in human peripheral blood lymphocytes.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 144 ·No. 8 ·1990-04-15 ·Pages 2891-8

Garrido MA, Perez P, Titus JA, Valdayo MJ, Winkler DF, Barbieri SA, Wunderlich JR, Segal DM

Abstract

We have isolated subsets of cells from human PBL and have investigated their abilities to mediate lysis targeted by bispecific antibodies. Targeted cytotoxic cells were divided into two distinct types based on buoyant density. The low buoyant density fraction contained all of the targetable cytotoxic activity in unstimulated PBL, including both T and K cells targeted with anti-CD3 and anti-Fc gamma RIII (CD16) containing bispecific antibodies, respectively. Both types of targetable cytotoxic cells required IL-2 for maintenance of cytotoxic activity, expressed the CD56 (NKH1) marker, and mediated MHC-unrestricted lysis. The targetable T cells in low density PBL were exclusively CD8+ and represented only about 2% of the total PBL. The high buoyant density lymphocytes, depleted of NK cells, had no targetable activity, but were able to generate over several days, targetable T cell activity in the presence of a TCR cross-linking signal plus IL-2. Unlike the low-density cells, the activated high buoyant density effector T cells did not express CD56, consisted of both CD4+ and CD8+ cells, and did not mediate MHC-unrestricted lysis. These cells proliferated more rapidly and generated more total lytic activity than the low-density fraction. Our studies show that targetable cytotoxic activity in human PBL is mediated by several subsets of cells with different activation requirements. Presumably all of these activities could be directed against unwanted cells in clinical or preclinical studies involving targeted cytotoxic cells.

MeSH Terms
Antigens, CD/analysis Antigens, Differentiation, T-Lymphocyte/analysis,immunology CD3 Complex CD4-Positive T-Lymphocytes/immunology CD56 Antigen CD8 Antigens Cell Separation Centrifugation, Density Gradient Cytotoxicity, Immunologic Flow Cytometry Immunity, Cellular Interleukin-2/pharmacology Killer Cells, Natural/immunology Lymphocyte Activation Receptor Aggregation Receptors, Antigen, T-Cell/immunology T-Lymphocytes, Cytotoxic/immunology
Chemicals
Antigens, CD Antigens, Differentiation, T-Lymphocyte CD3 Complex CD56 Antigen CD8 Antigens Interleukin-2 Receptors, Antigen, T-Cell
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Garrido M A
Experimental Immunology Branch, National Cancer Institute, Bethesda, MD 20892.
Perez P
Titus J A
Valdayo M J
Winkler D F
Barbieri S A
Wunderlich J R
Segal D M
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1990-04-15
Pages
2891-8
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
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