Skip to search boxSkip to navigationSkip to main content

Eradication of B-lineage cells and regression of lymphoma in a patient treated with autologous T cells genetically engineered to recognize CD19

  • James N. Kochenderfer
    ,
  • Wyndham H. Wilson
    ,
  • John E. Janik
    ,
  • Mark E. Dudley
    ,
  • Maryalice Stetler-Stevenson
    ,
  • Steven A. Feldman
  • National Institutes of Health
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Adoptive transfer of genetically modified T cells is an attractive approach for generating antitumor immune responses. We treated a patient with advanced follicular lymphoma by administering a preparative chemotherapy regimen followed by autologous T cells genetically engineered to express a chimeric antigen receptor (CAR) that recognized the B-cell antigen CD19. The patient's lymphoma underwent a dramatic regression, and B-cell precursors were selectively eliminated from the patient's bone marrow after infusion of anti - CD19-CAR-transduced T cells. Blood B cells were absent for at least 39 weeks after anti - CD19-CAR-transduced T-cell infusion despite prompt recovery of other blood cell counts. Consistent with eradication of B-lineage cells, serum immunoglobulins decreased to very low levels after treatment. The prolonged and selective elimination of Blineage cells could not be attributed to the chemotherapy that the patient received and indicated antigen-specific eradication of B-lineage cells. Adoptive transfer of anti - CD19-CAR-expressing T cells is a promising new approach for treating B-cell malignancies. This study is registered at www.clinicaltrials.gov as #NCT00924326.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 4099-4102 (4 pages)

Journal (Volume, Issue Number)

Blood (Volume 116, Issue 20)

Publication milestones

  • Published - 11/18/2010

Publication status

Published - 11/18/2010

ISSN

0006-4971

Publication IDs

  • Scopus: 78549278144
  • PubMed: 20668228

Publication metrics

Metrics

SciVal
FWCI
12.47
SciVal
Author count
12
SciVal
citations
843
SciVal
Paper percentile
99
SciVal
Top percentile
1
Fractional count
1
Fractional count
0.08
Fractional count
11
Fractional count
0.92
Fractional count
1
Fractional count
1
Scopus
citations

PlumX, opens in new tab

Citation count
1238
Social media
34
Mentions
8
Captures
1068

Funding Details

FunderFunding number
NCI
ZIABC011413