Follicular Lymphoma Microenvironment Characteristics Associated with Tumor Cell Mutations and MHC Class II Expression

Author:

Han Guangchun1ORCID,Deng Qing2ORCID,Marques-Piubelli Mario L.3ORCID,Dai Enyu1ORCID,Dang Minghao1ORCID,Ma Man Chun John2ORCID,Li Xubin2ORCID,Yang Haopeng2ORCID,Henderson Jared2ORCID,Kudryashova Olga4ORCID,Meerson Mark4ORCID,Isaev Sergey4ORCID,Kotlov Nikita4ORCID,Nomie Krystle J.4ORCID,Bagaev Alexander4ORCID,Parra Edwin R.5ORCID,Solis Soto Luisa M.5ORCID,Parmar Simrit2ORCID,Hagemeister Fredrick B.2ORCID,Ahmed Sairah2ORCID,Iyer Swaminathan P.2ORCID,Samaniego Felipe2ORCID,Steiner Raphael2ORCID,Fayad Luis2ORCID,Lee Hun2ORCID,Fowler Nathan H.24ORCID,Flowers Christopher R.2ORCID,Strati Paolo2ORCID,Westin Jason R.2ORCID,Neelapu Sattva S.2ORCID,Nastoupil Loretta J.2ORCID,Vega Francisco3ORCID,Wang Linghua16ORCID,Green Michael R.1267ORCID

Affiliation:

1. 1Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.

2. 2Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, Texas.

3. 3Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

4. 4BostonGene Corporation, Waltham, Massachusetts.

5. 5Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

6. 6UTHealth Graduate School of Biomedical Sciences, The University of Texas MD Anderson Cancer Center, Houston, Texas.

7. 7Center for Cancer Epigenetics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Abstract

Abstract Follicular lymphoma (FL) is a B-cell malignancy with a complex tumor microenvironment that is rich in nonmalignant immune cells. We applied single-cell RNA sequencing to characterize the diverse tumor and immune cell populations of FL and identified major phenotypic subsets of FL T cells, including a cytotoxic CD4 T-cell population. We characterized four major FL subtypes with differential representation or relative depletion of distinct T-cell subsets. By integrating exome sequencing, we observed that somatic mutations are associated with, but not definitive for, reduced MHC expression on FL cells. In turn, expression of MHCII genes by FL cells was associated with significant differences in the proportions and targetable immunophenotypic characteristics of T cells. This provides a classification framework of the FL microenvironment in association with FL genotypes and MHC expression, and informs different potential immunotherapeutic strategies based upon tumor cell MHCII expression. Significance: We have characterized the FL-infiltrating T cells, identified cytotoxic CD4 T cells as an important component that is associated with tumor cell–intrinsic characteristics, and identified sets of targetable immune checkpoints on T cells that differed from FLs with normal versus low MHC expression. See related commentary by Melnick, p. 374. This article is highlighted in the In This Issue feature, p. 369

Funder

National Cancer Institute

Leukemia and Lymphoma Society

Publisher

American Association for Cancer Research (AACR)

Subject

General Medicine

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