4.3 Review

Stimulation of anti-tumor immunity by photodynamic therapy

Journal

EXPERT REVIEW OF CLINICAL IMMUNOLOGY
Volume 7, Issue 1, Pages 75-91

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1586/ECI.10.81

Keywords

anti-tumor immunity; cancer vaccines; cytotoxic T-lymphocytes; damage-associated molecular patterns; dendritic cells; photodynamic therapy; Toll-like receptor agonists; tumor-associated antigens

Categories

Funding

  1. Partners Genzyme Translational Grant
  2. Swiss Science Foundation [205320-122144, IZLSZ2 _123011, 310030-119938, K-32K1-116460]
  3. NIH [R01AI050875]
  4. Center for Integration of Medicine and Innovative Technology [DAMD17-02-2-0006]
  5. CDMRP Program in TBI [W81XWH-09-1-0514]
  6. Air Force Office of Scientific Research [FA9950-04-1-0079]
  7. NATIONAL CANCER INSTITUTE [R01CA083882] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI050875] Funding Source: NIH RePORTER

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Photodynamic therapy (PDT) is a rapidly developing cancer treatment that utilizes the combination of nontoxic dyes and harmless visible light to destroy tumors by generating reactive oxygen species. PDT produces tumor-cell destruction in the context of acute inflammation that acts as a 'danger signal' to the innate immune system. Activation of the innate immune system increases the priming of tumor-specific T lymphocytes that have the ability to recognize and destroy distant tumor cells and, in addition, lead to the development of an immune memory that can combat recurrence of the cancer at a later point in time. PDT may be also successfully combined with immunomodulating strategies that are capable of overcoming or bypassing the escape mechanisms employed by the progressing tumor to evade immune attack. This article will cover the role of the immune response in PDT anti-tumor effectiveness. It will highlight the milestones in the development of PDT-mediated anti-tumor immunity and emphasize the combination strategies that may improve this therapy.

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