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Updated: May 27, 2026

Murine Model of CD40-activation of B cells
Published on: March 5, 2010
CD80 (B7.1) is expressed on both malignant B cells and nonmalignant stromal cells in non-Hodgkin lymphoma
Naveen Dakappagari1, Steffan N Ho, Randy D Gascoyne
1Global Clinical Assay Group, Pfizer, Inc, San Diego, California 92121, USA.
Insights
CD80 is expressed on malignant and nonmalignant cells in non-Hodgkin lymphoma (NHL). Targeting CD80 may modulate the tumor microenvironment, offering a new therapeutic strategy for NHL patients.
Area of Science:
- Immunology
- Oncology
- Hematology
Background:
- CD80, a B7 family immune coregulatory protein, mediates immune activation and suppression.
- CD80 interactions with B7-H1 support immune suppression.
- CD80 is a therapeutic target in non-Hodgkin lymphoma (NHL), with anti-CD80 antibodies showing efficacy.
Purpose of the Study:
- To define the potential of CD80 as a therapeutic target in NHL.
- To evaluate CD80 expression on malignant and nonmalignant cells in NHL.
Main Methods:
- Multicolor flow cytometric analysis.
- Evaluation of CD80 expression on primary lymphoma cell suspensions from 241 NHL biopsies.
Main Results:
- CD80 expressed on malignant B cells in follicular lymphoma (97%), diffuse large B-cell lymphoma (90%), marginal zone lymphoma (91%), mantle cell lymphoma (75%), and small lymphocytic lymphoma (43%).
- CD80 present on tumor-infiltrating T lymphocytes in nearly all cases.
- CD80 expressed by non-B, non-T cells in 68% (follicular) and 44% (diffuse large B-cell) NHL cases.
Conclusions:
- CD80 is expressed on both malignant and nonmalignant cells in NHL.
- Targeting CD80 can modulate intercellular interactions within the NHL tumor microenvironment.
Background:
CD80 is a member of the B7 family of immune coregulatory proteins that mediate both immune activation and suppression. CD80 in particular has recently been shown to play an important role in supporting immune suppression through interactions with B7-H1. CD80 has been identified as a therapeutic target in non-Hodgkin lymphoma (NHL) based on limited immunohistochemical studies of CD80 expression. Clinical studies have shown that the anti-CD80 antibody galiximab is safe and clinically efficacious in follicular NHL. However, the mechanisms through which targeting CD80 inhibits tumor progression remain poorly understood.
Methods:
To further define the potential of CD80 as a therapeutic target in NHL, CD80 expression was evaluated by multicolor flow cytometric analysis of primary lymphoma cell suspensions generated from 241 diagnostic biopsies of patients with NHL.
Results:
CD80 was expressed on malignant B cells in essentially all cases of follicular lymphoma (97%; n = 115), the majority of cases of diffuse large B-cell lymphoma (90%; n = 69), marginal zone lymphoma (91%; n = 22), mantle cell lymphoma (75%; n = 12), and in about half of small lymphocytic lymphoma cases (43%; n = 23). CD80 was also present on tumor-infiltrating T lymphocytes in nearly all cases. Additionally, CD80 was expressed by non-B, non-T cells in 68 and 44% of cases of follicular and diffuse large B-cell NHL, respectively.
Conclusions:
CD80 is expressed on both malignant cells and the nonmalignant cells in NHL. Therapeutic targeting of CD80 will therefore modulate the complex intercellular interactions that define the tumor microenvironment in NHL.
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