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Phase I Clinical Trial of Costimulated, IL-4 Polarized Donor CD4+ T Cells as Augmentation of Allogeneic Hematopoietic Cell Transplantation

  • Daniel H. Fowler(corresponding author)
    ,
  • Jeanne Odom
    ,
  • Seth M. Steinberg
    ,
  • Catherine K. Chow
    ,
  • Jason Foley
    ,
  • Yelena Kogan
*Corresponding author for this work
  • National Institutes of Health
    ,
  • National Institutes of Health, Bethesda
    ,
  • Rikshospitalet-Radiumhospitalet HF
    ,
  • University of Pennsylvania
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

The primary objective of this clinical trial was to evaluate the safety, feasibility, and biologic effects of administering costimulated, interleukin (IL)-4 polarized donor CD4+ T cells in the setting of HLA-matched sibling, T cell-replete allogeneic hematopoietic cell transplantation (HCT). Forty-seven subjects with hematologic malignancy received granulocyte colony-stimulating factor-mobilized allogeneic hematopoietic cell transplants and cyclosporine graft-versus-host disease (GVHD) prophylaxis after reduced intensity conditioning. Initial subjects received no additional cells (n = 19); subsequent subjects received additional donor CD4+ T cells generated ex vivo by CD3/CD28 costimulation in medium containing IL-4 and IL-2 (administered day 1 after HCT at 5, 25, or 125 × 106 cells/kg). Studies after HCT included measurement of monocyte IL-1α and tumor necrosis factor α, detection of T cells with antitumor specificity, and characterization of T cell cytokine phenotype. The culture method generated donor CD4+ T cells that secreted increased T helper 2 (Th2) cytokines and decreased T helper 1 (Th1) cytokines. Such Th2-like cells were administered without infusional or dose-limiting toxicity. The Th2 cohort had accelerated lymphocyte reconstitution; both cohorts had rapid hematopoietic recovery and alloengraftment. Acute GVHD and overall survival were similar in the Th2 and non-Th2 cohorts. Th2 cell recipients tended to have increased monocyte IL-1α and had increased tumor necrosis factor α secretion. CD8+ T cells with antitumor specificity were observed in Th2 and non-Th2 cohorts. Post-transplantation T cells from Th2 cell recipients secreted IL-4 and IL-10 (Th2 cytokines) and IL-2 and interferon γ (Th1 cytokines). Allograft augmentation with costimulated, IL-4-polarized donor CD4+ T cells resulted in activated Th1, Th2, and inflammatory cytokine pathways without an apparent increase in GVHD.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1150-1160 (11 pages)

Journal (Volume, Issue Number)

Biology of Blood and Marrow Transplantation (Volume 12, Issue 11)

Publication milestones

  • Published - 11/2006

Publication status

Published - 11/2006

ISSN

1083-8791

Publication IDs

  • Scopus: 33750511589
  • PubMed: 17085308

Publication metrics

Metrics

SciVal
FWCI
2.71
SciVal
Author count
21
SciVal
citations
53
SciVal
Paper percentile
88
Scopus
citations
Fractional count
1
Fractional count
0.05
Fractional count
20
Fractional count
0.95
Fractional count
1
Fractional count
1

PlumX, opens in new tab

Captures
15
Citation count
56

Funding Details

This work was supported in part by the Center for Cancer Research (D. Fowler, J. Odom, S. Steinberg, J. Foley, Y. Kogan, J. Hou, J. Gea-Banacloche, C. Sportes, S. Pavletic, R. Gress, and M. Bishop) and by a grant from the Leukemia and Lymphoma Society of America to the University of Pennsylvania Abramson Cancer Research Center (R. Fox, G. Beatty, R. Vonderheide, B. Levine, and C. June). The authors thank NIH Clinical Center, NIH Department of Transfusion Medicine, and NCI Pharmacy and Clinical Care Units for their dedication in providing care to patients on this study. They also acknowledge the contributions of Kate Castro, RN, Janine Daub, RN, Ladan Foruraghi, RN, Robert Dean, MD, Alan Wayne, MD, Frances Hakim, PhD, Barbara Vance, PhD, and Vicki Fellowes. This report is dedicated to the memory of Charles Carter as a great friend, colleague, and cell therapy pioneer in the wake of his untimely recent death.
FundersFunding numbers
Center for Cancer Research
-
University of Pennsylvania Abramson Cancer Research Center
-
LLS
-