Durable preservation of antiviral antibodies after CD19-directed chimeric antigen receptor T-cell immunotherapy

The long-term effects of CD19-targeted chimeric antigen receptor–modified T-cell immunotherapy (CD19-CARTx) for B-cell malignancies on humoral immunity are unclear. We examined antiviral humoral immunity in 39 adults with B-cell malignancies who achieved durable complete remission without additional...

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Veröffentlicht in:Blood advances 2019-11, Vol.3 (22), p.3590-3601
Hauptverfasser: Hill, Joshua A., Krantz, Elizabeth M., Hay, Kevin A., Dasgupta, Sayan, Stevens-Ayers, Terry, Bender Ignacio, Rachel A., Bar, Merav, Maalouf, Joyce, Cherian, Sindhu, Chen, Xueyan, Pepper, Greg, Riddell, Stanley R., Maloney, David G., Boeckh, Michael J., Turtle, Cameron J.
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Sprache:eng
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Zusammenfassung:The long-term effects of CD19-targeted chimeric antigen receptor–modified T-cell immunotherapy (CD19-CARTx) for B-cell malignancies on humoral immunity are unclear. We examined antiviral humoral immunity in 39 adults with B-cell malignancies who achieved durable complete remission without additional therapy for >6 months after CD19-CARTx. Despite CD19+ B-cell aplasia in all patients, the incidence of viral infections occurring >90 days post–CD19-CARTx was low (0.91 infections per person-year). Because long-lived plasma cells are CD19− and should not be direct targets of CD19-targeted chimeric antigen receptor T cells, we tested the hypothesis that humoral immunity was preserved after CD19-CARTx based on linear mixed-effects models of changes in serum total immunoglobulin G (IgG) concentration, measles IgG concentration, and the number of viruses or viral epitopes to which serum IgG was directed (the “antivirome”) using the novel VirScan assay. Samples were tested pre–CD19-CARTx and ∼1, 6, and 12 months post–CD19-CARTx. Although total IgG concentration was lower post–CD19-CARTx (mean change, −17.5%), measles IgG concentration was similar (mean change, 1.2%). Only 1 participant lost measles seroprotection post–CD19-CARTx but had undergone allogeneic hematopoietic cell transplantation before CD19-CARTx. The antivirome was also preserved, with mean absolute losses of 0.3 viruses and 6 viral epitopes detected between pre- and post–CD19-CARTx samples. Most participants gained IgG to ≥2 epitopes for ≥2 viruses, suggesting that humoral immunity to some viruses may be maintained or recover after successful CD19-CARTx. These findings may differ in children. Studies of immunoglobulin replacement and vaccination after CARTx are warranted. •Virus-specific IgG levels were stable for up to 1 year after CD19-CARTx in adults with durable complete remission.•Preexisting humoral immunity may be preserved in adult recipients of CD19-CARTx. [Display omitted]
ISSN:2473-9529
2473-9537
2473-9537
DOI:10.1182/bloodadvances.2019000717