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Double-negative (CD27 - IgD - ) B cells are expanded in NSCLC and inversely correlate with affinity-matured B cell populations

The presence of B cells in early stage non-small cell lung cancer (NSCLC) is associated with longer survival, however, the role these cells play in the generation and maintenance of anti-tumor immunity is unclear. B cells differentiate into a variety of subsets with differing characteristics and fun...

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Published in:Journal of translational medicine 2018-02, Vol.16 (1), p.30-30, Article 30
Main Authors: Centuori, Sara M, Gomes, Cecil J, Kim, Samuel S, Putnam, Charles W, Larsen, Brandon T, Garland, Linda L, Mount, David W, Martinez, Jesse D
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description The presence of B cells in early stage non-small cell lung cancer (NSCLC) is associated with longer survival, however, the role these cells play in the generation and maintenance of anti-tumor immunity is unclear. B cells differentiate into a variety of subsets with differing characteristics and functions. To date, there is limited information on the specific B cell subsets found within NSCLC. To better understand the composition of the B cell populations found in NSCLC we have begun characterizing B cells in lung tumors and have detected a population of B cells that are CD79A CD27 IgD . These CD27 IgD (double-negative) B cells have previously been characterized as unconventional memory B cells and have been detected in some autoimmune diseases and in the elderly population but have not been detected previously in tumor tissue. A total of 15 fresh untreated NSCLC tumors and 15 matched adjacent lung control tissues were dissociated and analyzed by intracellular flow cytometry to detect the B cell-related markers CD79A, CD27 and IgD. All CD79A B cells subsets were classified as either naïve (CD27 IgD ), affinity-matured (CD27 IgD ), early memory/germinal center cells (CD27 IgD ) or double-negative B cells (CD27 IgD ). Association of double-negative B cells with clinical data including gender, age, smoking status, tumor diagnosis and pathologic differentiation status were also examined using the logistic regression analysis for age and student's t-test for all other variables. Associations with other B cell subpopulations were examined using Spearman's rank correlation. We observed that double-negative B cells were frequently abundant in lung tumors compared to normal adjacent controls (13 out of 15 cases), and in some cases made up a substantial proportion of the total B cell compartment. The presence of double-negative cells was also found to be inversely related to the presence of affinity-matured B cells within the tumor, Spearman's coefficient of - 0.76. This study is the first to observe the presence of CD27 IgD double-negative B cells in human NSCLC and that this population is inversely correlated with traditional affinity-matured B cell populations.
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B cells differentiate into a variety of subsets with differing characteristics and functions. To date, there is limited information on the specific B cell subsets found within NSCLC. To better understand the composition of the B cell populations found in NSCLC we have begun characterizing B cells in lung tumors and have detected a population of B cells that are CD79A CD27 IgD . These CD27 IgD (double-negative) B cells have previously been characterized as unconventional memory B cells and have been detected in some autoimmune diseases and in the elderly population but have not been detected previously in tumor tissue. A total of 15 fresh untreated NSCLC tumors and 15 matched adjacent lung control tissues were dissociated and analyzed by intracellular flow cytometry to detect the B cell-related markers CD79A, CD27 and IgD. 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All CD79A B cells subsets were classified as either naïve (CD27 IgD ), affinity-matured (CD27 IgD ), early memory/germinal center cells (CD27 IgD ) or double-negative B cells (CD27 IgD ). Association of double-negative B cells with clinical data including gender, age, smoking status, tumor diagnosis and pathologic differentiation status were also examined using the logistic regression analysis for age and student's t-test for all other variables. Associations with other B cell subpopulations were examined using Spearman's rank correlation. We observed that double-negative B cells were frequently abundant in lung tumors compared to normal adjacent controls (13 out of 15 cases), and in some cases made up a substantial proportion of the total B cell compartment. The presence of double-negative cells was also found to be inversely related to the presence of affinity-matured B cells within the tumor, Spearman's coefficient of - 0.76. 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All CD79A B cells subsets were classified as either naïve (CD27 IgD ), affinity-matured (CD27 IgD ), early memory/germinal center cells (CD27 IgD ) or double-negative B cells (CD27 IgD ). Association of double-negative B cells with clinical data including gender, age, smoking status, tumor diagnosis and pathologic differentiation status were also examined using the logistic regression analysis for age and student's t-test for all other variables. Associations with other B cell subpopulations were examined using Spearman's rank correlation. We observed that double-negative B cells were frequently abundant in lung tumors compared to normal adjacent controls (13 out of 15 cases), and in some cases made up a substantial proportion of the total B cell compartment. The presence of double-negative cells was also found to be inversely related to the presence of affinity-matured B cells within the tumor, Spearman's coefficient of - 0.76. 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subjects Aged
Aged, 80 and over
Analysis
Antibody Affinity - immunology
B cells
B-Lymphocytes - pathology
Carcinoma, Non-Small-Cell Lung - immunology
Carcinoma, Non-Small-Cell Lung - pathology
CD27
Cell Proliferation
Diagnosis
Double-negative B cells
Female
Health aspects
Humans
Immunoglobulin D - metabolism
Lung cancer
Lung cancer, Non-small cell
Lung Neoplasms - immunology
Lung Neoplasms - pathology
Male
Middle Aged
NSCLC
TIL-Bs
Tumor Necrosis Factor Receptor Superfamily, Member 7 - metabolism
title Double-negative (CD27 - IgD - ) B cells are expanded in NSCLC and inversely correlate with affinity-matured B cell populations
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