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Herpes simplex virus lymphadenitis is associated with tumor reduction in a chronic lymphocytic leukemia patient

  1. Author:
    Chang, Andres
    Sholukh, Anton M
    Wieland, Andreas
    Jaye, David L
    Carrington,Mary
    Huang, Meei-Li
    Xie, Hong
    Jerome, Keith R
    Roychoudhury, Pavitra
    Greninger, Alexander L
    Koff, Jean L
    Cohen, Jonathon B
    Koelle, David M
    Corey, Lawrence
    Flowers, Christopher R
    Ahmed, Rafi
  2. Author Address

    Winship Cancer Institute of Emory University, Atlanta, United States of America., Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, United States of America., Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, United States of America., Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, United States of America., Laboratory of Experimental Immunology, Frederick National Laboratory for Cancer Research, Bethesda, United States of America., University of Washington, Seattle, United States of America., Department of Laboratory Medicine and Pathology, University of Washington, Seattle, United States of America., Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, United States of America., Department of Global Health, University of Washington, Seattle, United States of America., Department of Lymphoma and Myeloma, MD Anderson Cancer Center, Houston, United States of America.,
    1. Year: 2022
    2. Date: Jul 21
    3. Epub Date: 2022 07 21
  1. Journal: The Journal of Clinical Investigation
    1. 132
    2. 18
  2. Type of Article: Article
  3. Article Number: e161109
  1. Abstract:

    Herpes simplex virus lymphadenitis (HSVL) is an unusual presentation of HSV reactivation in chronic lymphocytic leukemia (CLL) patients characterized by systemic symptoms and no herpetic lesions. The immune responses during HSVL have not been studied. Peripheral blood and lymph node samples of a patient with HSVL were obtained. HSV-2 viral load, antibody levels, B and T cell responses, cytokine levels, and tumor burden were measured. This patient showed HSV-2 viremia for at least 6 weeks. During this period, she had a robust HSV-specific antibody response with neutralizing and antibody-dependent cellular phagocytosis activity. Activated (HLA-DR+, CD38+) CD4+ and CD8+ T cells increased 18-fold and HSV-specific CD8+ T cells were detected in the blood at higher numbers. HSV-specific B and T cell responses in the lymph node were also detected. Markedly elevated levels of pro-inflammatory cytokines in the blood were also observed. Surprisingly, a sustained decrease in CLL tumor burden without CLL-directed therapy was observed with this and also a prior episode of HSVL. HSVL should be considered as part of the differential diagnosis in CLL patients who present with signs and symptoms of aggressive lymphoma transformation. An interesting finding was the sustained tumor control after 2 episodes of HSVL in this patient. This tumor burden reduction may be due to the HSV-specific response serving as an adjuvant for activating tumor-specific or bystander T cells. Studies in additional CLL patients are needed to confirm and extend these findings. National Institutes of Health and Winship Cancer Institute.

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External Sources

  1. DOI: 10.1172/JCI161109
  2. PMID: 35862190
  3. WOS: 000880652000003
  4. PII : 161109

Library Notes

  1. Fiscal Year: FY2021-2022
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