CD1c but neither CD1a nor CD1b molecules are expressed on normal, activated, and malignant human B cells: Identification of a new B-cell subset

D. Delia, G. Cattoretti, N. Polli, E. Fontanella, A. Aiello, R. Giardini, F. Rilke, G. Della Porta

Research output: Contribution to journalArticle

Abstract

The CD1 cluster of monoclonal antibodies (MoAbs) CD1a, CD1b, and CD1c, identifies molecules that are differentially expressed on hematopoietic and nonhematopoietic tissues. Our earlier finding that the mantle zone (MZ) but not the germinal center (GC) of normal lymph nodes (LN) is CD1c+, CD1a-, and CD1b- prompted us to further investigate the expresion of these molecules on normal, activated, and malignant B cells. We report that blood and spleen contain CD1c+ B cells that account for 49% ± 20.4% (mean ± SD) and 50.9% ± 4.4% of the total B cell population, respectively. CD1a- and CD1b-specific MoAbs are unreactive with both B and T cells; these latter are CD1c- as well. When CD1c+ and CD1c- B cells are activated in vitro, the CD1c molecule is upregulated in the former subset and induced de novo in the latter. Conversely, activated blood T cells remain CD1c-. Neither CD1a nor CD1b molecules are detected on activated T and B lymphocytes. At ultrastructural level, the CD1c+ B cells exhibit distinctive features, namely, condensed chromatin with or without a nucleolus and a unique cluster of cytoplasmic vesicles and organelles; the number of nucleolated cells is higher in the spleen (95%) than in the tonsil (40%) or blood (5%). These findings further confirm the similarity between blood and MZ B cells. The CD1c expression assessed on 27 B-cell chronic lymphocytic leukemias (B-CLL) and 46 B non-Hodgkin's lymphomas (B-NHL) was detected on 41% and 32% of cases, respectively; the latter comprised four follicular and 11 diffuse histotypes. The Burkitt's lymphomas were CD1c-negative. The B-cell neoplasms were all CD1a- and, except for four with a weak cytoplasmic staining, all CD1b- as well. The clear-cut CD1c distribution in normal LN (MZ+, GC-) contrasted with the evidence that some B-NHL cells of GC origin (eg, follicular with predominantly small cleaved cells), were CD1c+. Overall, the finding that CD1c expression is restricted to a fraction of B cells present in lymphoid organs and in peripheral blood indicates that CD1c is a powerful marker for the identification and dissection of B-cell subsets whose functional properties can now be evaluated.

Original languageEnglish
Pages (from-to)241-247
Number of pages7
JournalBlood
Volume72
Issue number1
Publication statusPublished - 1988

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B-Lymphocyte Subsets
B-Lymphocytes
Cells
Molecules
Blood
Germinal Center
T-cells
T-Lymphocytes
Non-Hodgkin's Lymphoma
Spleen
Lymph Nodes
Monoclonal Antibodies
Cytoplasmic Vesicles
Dissection
Burkitt Lymphoma
Lymphocytes
Palatine Tonsil
Normal Distribution
B-Cell Chronic Lymphocytic Leukemia
Organelles

ASJC Scopus subject areas

  • Hematology

Cite this

Delia, D., Cattoretti, G., Polli, N., Fontanella, E., Aiello, A., Giardini, R., ... Della Porta, G. (1988). CD1c but neither CD1a nor CD1b molecules are expressed on normal, activated, and malignant human B cells: Identification of a new B-cell subset. Blood, 72(1), 241-247.

CD1c but neither CD1a nor CD1b molecules are expressed on normal, activated, and malignant human B cells : Identification of a new B-cell subset. / Delia, D.; Cattoretti, G.; Polli, N.; Fontanella, E.; Aiello, A.; Giardini, R.; Rilke, F.; Della Porta, G.

In: Blood, Vol. 72, No. 1, 1988, p. 241-247.

Research output: Contribution to journalArticle

Delia, D, Cattoretti, G, Polli, N, Fontanella, E, Aiello, A, Giardini, R, Rilke, F & Della Porta, G 1988, 'CD1c but neither CD1a nor CD1b molecules are expressed on normal, activated, and malignant human B cells: Identification of a new B-cell subset', Blood, vol. 72, no. 1, pp. 241-247.
Delia, D. ; Cattoretti, G. ; Polli, N. ; Fontanella, E. ; Aiello, A. ; Giardini, R. ; Rilke, F. ; Della Porta, G. / CD1c but neither CD1a nor CD1b molecules are expressed on normal, activated, and malignant human B cells : Identification of a new B-cell subset. In: Blood. 1988 ; Vol. 72, No. 1. pp. 241-247.
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abstract = "The CD1 cluster of monoclonal antibodies (MoAbs) CD1a, CD1b, and CD1c, identifies molecules that are differentially expressed on hematopoietic and nonhematopoietic tissues. Our earlier finding that the mantle zone (MZ) but not the germinal center (GC) of normal lymph nodes (LN) is CD1c+, CD1a-, and CD1b- prompted us to further investigate the expresion of these molecules on normal, activated, and malignant B cells. We report that blood and spleen contain CD1c+ B cells that account for 49{\%} ± 20.4{\%} (mean ± SD) and 50.9{\%} ± 4.4{\%} of the total B cell population, respectively. CD1a- and CD1b-specific MoAbs are unreactive with both B and T cells; these latter are CD1c- as well. When CD1c+ and CD1c- B cells are activated in vitro, the CD1c molecule is upregulated in the former subset and induced de novo in the latter. Conversely, activated blood T cells remain CD1c-. Neither CD1a nor CD1b molecules are detected on activated T and B lymphocytes. At ultrastructural level, the CD1c+ B cells exhibit distinctive features, namely, condensed chromatin with or without a nucleolus and a unique cluster of cytoplasmic vesicles and organelles; the number of nucleolated cells is higher in the spleen (95{\%}) than in the tonsil (40{\%}) or blood (5{\%}). These findings further confirm the similarity between blood and MZ B cells. The CD1c expression assessed on 27 B-cell chronic lymphocytic leukemias (B-CLL) and 46 B non-Hodgkin's lymphomas (B-NHL) was detected on 41{\%} and 32{\%} of cases, respectively; the latter comprised four follicular and 11 diffuse histotypes. The Burkitt's lymphomas were CD1c-negative. The B-cell neoplasms were all CD1a- and, except for four with a weak cytoplasmic staining, all CD1b- as well. The clear-cut CD1c distribution in normal LN (MZ+, GC-) contrasted with the evidence that some B-NHL cells of GC origin (eg, follicular with predominantly small cleaved cells), were CD1c+. Overall, the finding that CD1c expression is restricted to a fraction of B cells present in lymphoid organs and in peripheral blood indicates that CD1c is a powerful marker for the identification and dissection of B-cell subsets whose functional properties can now be evaluated.",
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T1 - CD1c but neither CD1a nor CD1b molecules are expressed on normal, activated, and malignant human B cells

T2 - Identification of a new B-cell subset

AU - Delia, D.

AU - Cattoretti, G.

AU - Polli, N.

AU - Fontanella, E.

AU - Aiello, A.

AU - Giardini, R.

AU - Rilke, F.

AU - Della Porta, G.

PY - 1988

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N2 - The CD1 cluster of monoclonal antibodies (MoAbs) CD1a, CD1b, and CD1c, identifies molecules that are differentially expressed on hematopoietic and nonhematopoietic tissues. Our earlier finding that the mantle zone (MZ) but not the germinal center (GC) of normal lymph nodes (LN) is CD1c+, CD1a-, and CD1b- prompted us to further investigate the expresion of these molecules on normal, activated, and malignant B cells. We report that blood and spleen contain CD1c+ B cells that account for 49% ± 20.4% (mean ± SD) and 50.9% ± 4.4% of the total B cell population, respectively. CD1a- and CD1b-specific MoAbs are unreactive with both B and T cells; these latter are CD1c- as well. When CD1c+ and CD1c- B cells are activated in vitro, the CD1c molecule is upregulated in the former subset and induced de novo in the latter. Conversely, activated blood T cells remain CD1c-. Neither CD1a nor CD1b molecules are detected on activated T and B lymphocytes. At ultrastructural level, the CD1c+ B cells exhibit distinctive features, namely, condensed chromatin with or without a nucleolus and a unique cluster of cytoplasmic vesicles and organelles; the number of nucleolated cells is higher in the spleen (95%) than in the tonsil (40%) or blood (5%). These findings further confirm the similarity between blood and MZ B cells. The CD1c expression assessed on 27 B-cell chronic lymphocytic leukemias (B-CLL) and 46 B non-Hodgkin's lymphomas (B-NHL) was detected on 41% and 32% of cases, respectively; the latter comprised four follicular and 11 diffuse histotypes. The Burkitt's lymphomas were CD1c-negative. The B-cell neoplasms were all CD1a- and, except for four with a weak cytoplasmic staining, all CD1b- as well. The clear-cut CD1c distribution in normal LN (MZ+, GC-) contrasted with the evidence that some B-NHL cells of GC origin (eg, follicular with predominantly small cleaved cells), were CD1c+. Overall, the finding that CD1c expression is restricted to a fraction of B cells present in lymphoid organs and in peripheral blood indicates that CD1c is a powerful marker for the identification and dissection of B-cell subsets whose functional properties can now be evaluated.

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