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New research · Hematology
Blood advances · 23h
StudyBlood advances · 2026

Proteomic and proteogenomic identification of targetable T-cell antigens in multiple myeloma.

Gabriela Zuleger, Niklas de Andrade Krätzig, Piero Giansanti … Angela Krackhardt
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HematologyStudy

About 30% of multiple myeloma cell line peptides elicited CD8+ T-cell responses.

Proteomic and proteogenomic identification of targetable T-cell antigens in multiple myeloma.

Gabriela Zuleger et al. · Blood advances · 2026
Results
About 30% of peptides from multiple myeloma cell lines stimulated CD8+ T-cell responses.
n = 8
More results

Multiple myeloma (MM) accounts for approximately 12% of all hematologic malignancies and remains incurable despite therapeutic advances.

However, knowledge of targetable tumor antigens, especially neoantigens, is limited.

More results

We applied a mass spectrometry (MS)-based immunopeptidomics approach on primary MM samples (n = 8) and MM cell lines (n = 3), integrating whole-exome and RNA sequencing to comprehensively characterize the MM immunopeptidome and systematically search for TAAs and neoantigens.

“
Conclusion

This study provides the first proteogenomic-based identification of neoantigens in MM, extends the observation of presented Ig-derived neoantigens from B cell lymphoma to MM, and highlights both actionable antigens and barriers to effective TCR-based immunotherapy.

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