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Immunostimulatory effects of melphalan and usefulness in adoptive cell therapy with antitumor CD4+ t cells

  • Michal Kuczma
    ,
  • Zhi Chun Ding
    ,
  • Gang Zhou(corresponding author)
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

The alkylating agent melphalan is used in the treatment of hematological malignancies, especially multiple myeloma. In the past, the usefulness of melphalan has been solely attributed to its cytotoxicity on fastgrowing cancerous cells. Although the immunomodulatory effects of melphalan were suggested many years ago, only recently has this aspect of melphalan’s activity begun to be elucidated at the molecular level. Emerging evidence indicates that melphalan can foster an immunogenic microenvironment by inducing immunogenic cell death (ICD) as characterized by membrane translocation of endoplasmic reticulum protein calreticulin (CRT) and by release of chromatin-binding protein high-mobility group box 1 (HMGB1). In addition, the lympho-depletive effect of melphalan can induce the release of pro-inflammatory cytokines and growth factors, deplete regulatory T cells, and create space to facilitate the expansion of infused tumor-reactive T cells. These features suggest that melphalan can be used as a preparative chemotherapy for adoptive T-cell therapy. This notion is supported by our recent work demonstrating that the combination of melphalan and adoptive transfer of tumor-reactive CD4+ T cells can mediate potent antitumor effects in animal models. This review summarizes the recent advances in understanding and utilizing the immunomodulatory effects of melphalan.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 179-191 (13 pages)

Journal (Volume, Issue Number)

Critical Reviews in Immunology (Volume 36, Issue 2)

Publication milestones

  • Published - 2016

Publication status

Published - 2016

ISSN

1040-8401

Publication IDs

  • Scopus: 84994403320
  • PubMed: 27910767

Publication metrics

Metrics

Scopus
citations
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
1
SciVal
FWCI
0.08
SciVal
Author count
3
SciVal
citations
12
SciVal
Paper percentile
76

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Citation count
31
Captures
39

Funding Details

The authors thank members of the Zhou Laboratory for insightful discussions. This work is funded by National Institutes of HealthNIH grant R01CA158202 and the American Cancer Society Research Scholar Grant (RSG-12-169-01-LIB) to G.Z.
FundersFunding numbers
NIH
-
ACS
RSG-12-169-01-LIB
NCI
R01CA158202