Home LiteratureArticle Details
PMID: 2960766 Published · ppublish English Journal Article

The activation of L3T4+ helper T cells assisting the generation of anti-tumor Lyt-2+ cytotoxic T lymphocytes: requirement of Ia-positive antigen-presenting cells for processing and presentation of tumor antigens.

Journal of leukocyte biology ·Vol. 42 ·No. 6 ·1987-12-00 ·Pages 632-41

Kosugi A, Yoshioka T, Suda T, Sano H, Takahama Y, Fujiwara H, Hamaoka T

Abstract

The present study investigates the mechanisms of the recognition of tumor antigens by L3T4+ helper T cells responsible for the generation of Lyt-2+ cytotoxic T lymphocytes (CTL) against a major histocompatibility complex (MHC) Class II (Ia) antigen-negative syngeneic X5563 plasmacytoma. Treatment of X5563-immunized spleen cells with anti-L3T4 antibody plus complement (C) diminished the generation of Lyt-2+ anti-X5563 CTL. Since the contribution of L3T4+ cells was completely replaced by the addition of exogenous lymphokines, it was demonstrated that L3T4+ cells functioned as helper T cells assisting the generation of anti-X5563 CTL responses. Elimination of Ia-positive accessory cells (AC) from X5563-immunized spleen cells resulted in the abrogation of CTL generation, whereas the addition of exogenous lymphokines to AC-depleted X5563 immunized spleen cells restored the CTL response. The addition of anti-self Ia antibody to the culture also eliminated CTL responses. These observations demonstrated the requirement of Ia-positive AC for and the involvement of self Ia antigens in the activation of helper T cells. Moreover, use of tumor cells pretreated with paraformaldehyde to cultures of X5563-immunized spleen cells or adding back of AC pretreated with chloroquine to cultures of AC-depleted immune spleen cells failed to generate CTL responses. Finally, the addition of exogenous lymphokines to the above cultures resulted in appreciable restoration of CTL responses. Taken collectively, these results indicate that L3T4+ helper T cells are activated with tumor antigens processed and presented by Ia-positive AC.

MeSH Terms
Animals Antigen-Presenting Cells/drug effects,immunology Antigens, Neoplasm/immunology Chloroquine/pharmacology Female Histocompatibility Antigens Class II/immunology Lymphocyte Activation Lymphokines/pharmacology Mice Mice, Inbred C3H Mice, Inbred C57BL Plasmacytoma/immunology Radiation Chimera Spleen/transplantation T-Lymphocytes, Cytotoxic/immunology T-Lymphocytes, Helper-Inducer/immunology
Chemicals
Antigens, Neoplasm Histocompatibility Antigens Class II Lymphokines Chloroquine
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Kosugi A
Department of Oncogenesis, Osaka University Medical School, Japan.
Yoshioka T
Suda T
Sano H
Takahama Y
Fujiwara H
Hamaoka T
Article Info
Journal
Journal of leukocyte biology
Abbr.
J Leukoc Biol
ISSN
0741-5400
Published
1987-12-00
Pages
632-41
Language
English
Region
United States
NLM ID
8405628
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]