Patients with Multiple Myeloma Develop SOX2-Specific Autoantibodies after Allogeneic Stem Cell Transplantation

Author:

Kobold Sebastian123,Tams Sinje12,Luetkens Tim12,Cao Yanran12,Sezer Orhan12,Bartels Britta Marlen12,Reinhard Henrike12,Templin Julia12,Bartels Katrin12,Hildebrandt York4,Lajmi Nesrine12,Marx Andreas5,Haag Friedrich6,Bokemeyer Carsten12,Kröger Nicolaus4,Atanackovic Djordje12

Affiliation:

1. Department of Internal Medicine II, Oncology/Hematology/Bone Marrow Transplantation with the Section Pneumology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany

2. University Cancer Center Hamburg (Hubertus Wald Tumorzentrum), University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany

3. Division of Clinical Pharmacology, Department of Internal Medicine, Ludwig-Maximilian University, 80336 Munich, Germany

4. Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany

5. Institute for Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany

6. Institute for Immunology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany

Abstract

The occurrence of SOX2-specific autoantibodies seems to be associated with an improved prognosis in patients with monoclonal gammopathy of undetermined significance (MGUS). However, it is unclear if SOX2-specific antibodies also develop in established multiple myeloma (MM). Screening 1094 peripheral blood (PB) sera from 196 MM patients and 100 PB sera from healthy donors, we detected SOX2-specific autoantibodies in 7.7% and 2.0% of patients and donors, respectively. We identified SOX2211–230as an immunodominant antibody-epitope within the full protein sequence. SOX2 antigen was expressed in most healthy tissues and its expression did not correlate with the number of BM-resident plasma cells. Accordingly, anti-SOX2 immunity was not related to SOX2 expression levels or tumor burden in the patients’ BM. The only clinical factor predicting the development of anti-SOX2 immunity was application of allogeneic stem cell transplantation (alloSCT). Anti-SOX2 antibodies occurred more frequently in patients who had received alloSCT (n=74). Moreover, most SOX2-seropositive patients had only developed antibodies after alloSCT. This finding indicates that alloSCT is able to break tolerance towards this commonly expressed antigen. The questions whether SOX2-specific autoantibodies merely represent an epiphenomenon, are related to graft-versus-host effects or participate in the immune control of myeloma needs to be answered in prospective studies.

Funder

Erich und Gertrud Roggenbuck-Stiftung

Publisher

Hindawi Limited

Subject

General Medicine,Immunology,Immunology and Allergy

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