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Differential signaling via surface IgM is associated with VH gene mutational status and CD38 expression in chronic lymphocytic leukemia

Differential signaling via surface IgM is associated with VH gene mutational status and CD38 expression in chronic lymphocytic leukemia
Differential signaling via surface IgM is associated with VH gene mutational status and CD38 expression in chronic lymphocytic leukemia
The mutational status of tumor immunoglobulin VH genes is providing a powerful prognostic marker for chronic lymphocytic leukemia (CLL), with patients having tumors expressing unmutated VH genes being in a less favorable subset. However, the biologic differences correlating with VH gene status that could determine the clinical course of the disease are unknown. Here we show that differing responses to IgM ligation are closely associated with VH gene status. Specifically, 80% of cases with unmutated VH genes showed increased global tyrosine phosphorylation following IgM ligation, whereas only 20% of samples with mutated VH genes responded (P = .0002). There was also an association between response to IgM ligation and expression of CD38 (P = .015). The Syk kinase, critical for transducing B-cell receptor (BCR)- derived signals, was constitutively present in all CLL samples, and there was a perfect association between global phosphorylation and induction of phosphorylation/activation of Syk. Nonresponsiveness to anti-IgM could be circumvented by ligation of IgD (10 of 15 samples tested) or the BCR-associated molecule CD79alpha (12 of 15 samples tested). These results suggest that multiple mechanisms underlie nonresponsiveness to anti-IgM in CLL and that retained responsiveness to anti-IgM contributes to the poor prognosis associated with the unmutated subset of CLL. The prognostic power of the in vitro response to IgM ligation remains to be determined in a large series, but the simple technology involved may present an alternative or additional test for predicting clinical course.
0006-4971
1087-1093
Lanham, Stuart
28fdbbef-e3b6-4fdf-bd0f-4968eeb614d6
Hamblin, Terry
d1c0d3d4-8ce7-41c1-a5a5-055b72ad073e
Oscier, David
c2620a1d-25bb-48f7-9651-f5d023636381
Ibbotson, Rachel
7c121fe4-8501-44be-abf7-55f81a8b66a2
Stevenson, Freda
ba803747-c0ac-409f-a9c2-b61fde009f8c
Packham, Graham
fdabe56f-2c58-469c-aadf-38878f233394
Lanham, Stuart
28fdbbef-e3b6-4fdf-bd0f-4968eeb614d6
Hamblin, Terry
d1c0d3d4-8ce7-41c1-a5a5-055b72ad073e
Oscier, David
c2620a1d-25bb-48f7-9651-f5d023636381
Ibbotson, Rachel
7c121fe4-8501-44be-abf7-55f81a8b66a2
Stevenson, Freda
ba803747-c0ac-409f-a9c2-b61fde009f8c
Packham, Graham
fdabe56f-2c58-469c-aadf-38878f233394

Lanham, Stuart, Hamblin, Terry, Oscier, David, Ibbotson, Rachel, Stevenson, Freda and Packham, Graham (2003) Differential signaling via surface IgM is associated with VH gene mutational status and CD38 expression in chronic lymphocytic leukemia. Blood, 101 (3), 1087-1093. (doi:10.1182/blood-2002-06-1822).

Record type: Article

Abstract

The mutational status of tumor immunoglobulin VH genes is providing a powerful prognostic marker for chronic lymphocytic leukemia (CLL), with patients having tumors expressing unmutated VH genes being in a less favorable subset. However, the biologic differences correlating with VH gene status that could determine the clinical course of the disease are unknown. Here we show that differing responses to IgM ligation are closely associated with VH gene status. Specifically, 80% of cases with unmutated VH genes showed increased global tyrosine phosphorylation following IgM ligation, whereas only 20% of samples with mutated VH genes responded (P = .0002). There was also an association between response to IgM ligation and expression of CD38 (P = .015). The Syk kinase, critical for transducing B-cell receptor (BCR)- derived signals, was constitutively present in all CLL samples, and there was a perfect association between global phosphorylation and induction of phosphorylation/activation of Syk. Nonresponsiveness to anti-IgM could be circumvented by ligation of IgD (10 of 15 samples tested) or the BCR-associated molecule CD79alpha (12 of 15 samples tested). These results suggest that multiple mechanisms underlie nonresponsiveness to anti-IgM in CLL and that retained responsiveness to anti-IgM contributes to the poor prognosis associated with the unmutated subset of CLL. The prognostic power of the in vitro response to IgM ligation remains to be determined in a large series, but the simple technology involved may present an alternative or additional test for predicting clinical course.

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Published date: 2003

Identifiers

Local EPrints ID: 26430
URI: http://eprints.soton.ac.uk/id/eprint/26430
ISSN: 0006-4971
PURE UUID: e4451381-d996-4a3b-94a3-fc0d26133377
ORCID for Stuart Lanham: ORCID iD orcid.org/0000-0002-4516-264X
ORCID for Freda Stevenson: ORCID iD orcid.org/0000-0002-0933-5021
ORCID for Graham Packham: ORCID iD orcid.org/0000-0002-9232-5691

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Date deposited: 19 Apr 2006
Last modified: 16 Mar 2024 03:14

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Contributors

Author: Stuart Lanham ORCID iD
Author: Terry Hamblin
Author: David Oscier
Author: Rachel Ibbotson
Author: Freda Stevenson ORCID iD
Author: Graham Packham ORCID iD

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