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Single-cell profiling reveals the importance of CXCL13/CXCR5 axis biology in lymphocyte-rich classic Hodgkin lymphoma.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2021 Oct 12; Vol. 118 (41). - Publication Year :
- 2021
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Abstract
- Lymphocyte-rich classic Hodgkin lymphoma (LR-CHL) is a rare subtype of Hodgkin lymphoma. Recent technical advances have allowed for the characterization of specific cross-talk mechanisms between malignant Hodgkin Reed-Sternberg (HRS) cells and different normal immune cells in the tumor microenvironment (TME) of CHL. However, the TME of LR-CHL has not yet been characterized at single-cell resolution. Here, using single-cell RNA sequencing (scRNA-seq), we examined the immune cell profile of 8 cell suspension samples of LR-CHL in comparison to 20 samples of the mixed cellularity (MC, 9 cases) and nodular sclerosis (NS, 11 cases) subtypes of CHL, as well as 5 reactive lymph node controls. We also performed multicolor immunofluorescence (MC-IF) on tissue microarrays from the same patients and an independent validation cohort of 31 pretreatment LR-CHL samples. ScRNA-seq analysis identified a unique CD4 <superscript>+</superscript> helper T cell subset in LR-CHL characterized by high expression of Chemokine C-X-C motif ligand 13 (CXCL13) and PD-1. PD-1 <superscript>+</superscript> CXCL13 <superscript>+</superscript> T cells were significantly enriched in LR-CHL compared to other CHL subtypes, and spatial analyses revealed that in 46% of the LR-CHL cases these cells formed rosettes surrounding HRS cells. MC-IF analysis revealed CXCR5 <superscript>+</superscript> normal B cells in close proximity to CXCL13 <superscript>+</superscript> T cells at significantly higher levels in LR-CHL. Moreover, the abundance of PD-1 <superscript>+</superscript> CXCL13 <superscript>+</superscript> T cells in the TME was significantly associated with shorter progression-free survival in LR-CHL ( P = 0.032). Taken together, our findings strongly suggest the pathogenic importance of the CXCL13/CXCR5 axis and PD-1 <superscript>+</superscript> CXCL13 <superscript>+</superscript> T cells as a treatment target in LR-CHL.<br />Competing Interests: Competing interest statement: C.S. has performed consultancy for Seattle Genetics, Curis Inc., Roche, AbbVie, Juno Therapeutics, and Bayer and has received research funding from Bristol-Myers Squibb, Epizyme, and Trillium Therapeutics Inc. C.S. and D.W.S. are coinventors on a patent (“Method for determining lymphoma type”) using NanoString technology. D.W.S. has performed consultancy for Abbvie, AstraZeneca, Celgene, and Janssen and has received research funding from Janssen, NanoString, and Roche.<br /> (Copyright © 2021 the Author(s). Published by PNAS.)
- Subjects :
- B7-H1 Antigen metabolism
Fluorescent Antibody Technique
Humans
Lymph Nodes cytology
Programmed Cell Death 1 Receptor metabolism
RNA-Seq
Reed-Sternberg Cells pathology
Single-Cell Analysis
Tumor Microenvironment immunology
B-Lymphocytes metabolism
Chemokine CXCL13 metabolism
Hodgkin Disease pathology
Receptors, CXCR5 metabolism
T-Lymphocytes, Helper-Inducer metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 118
- Issue :
- 41
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 34615710
- Full Text :
- https://doi.org/10.1073/pnas.2105822118