Role of CD68 in the tumor immune microenvironment in Hodgkin's lymphoma

Valeria Tomarchio1, Luigi Rigacci1,2

  • 1Fondazione Policlinico Universitario Campus Bio-Medico, Roma, Italy.

PubMed

Insights

High CD68 macrophage infiltration in classical Hodgkin Lymphoma (cHL) indicates poor prognosis and aids in identifying high-risk patients. Targeting these macrophages may offer new therapeutic strategies for refractory disease.

Area of Science:

  • Oncology
  • Immunology
  • Hematology

Background:

  • Classical Hodgkin Lymphoma (cHL) has a high cure rate, but refractory cases pose treatment challenges.
  • Reed Sternberg Cells (HRSC) are central to cHL, but the tumor microenvironment significantly influences disease progression.
  • Immune cell interactions, chemokines, and cytokines within the tumor microenvironment are critical for cHL pathogenesis.

Purpose of the Study:

  • To review the literature on the role of CD68 macrophages in classical Hodgkin Lymphoma.
  • To examine the interaction between CD68 macrophages, HRSC, and the cHL milieu.
  • To discuss the clinical impact and therapeutic potential of targeting CD68 macrophages in cHL.

Main Methods:

  • Literature review of current significant studies on CD68 macrophages in cHL.
  • Analysis of the protumor role of CD68 macrophages in supporting HRSC survival.
  • Examination of the correlation between CD68 macrophage infiltration and patient prognosis.

Main Results:

  • CD68+ macrophages act as 'protumor' cells, supporting HRSC survival via cell-to-cell and paracrine interactions.
  • Increased infiltration of CD68 macrophages is associated with a poorer prognosis in cHL patients.
  • The review provides an updated perspective on CD68 macrophages in cHL, highlighting their clinical significance.

Conclusions:

  • Elevated baseline CD68 macrophages in cHL patients can identify high-risk individuals and inform treatment decisions for refractory disease.
  • Macrophage-targeted strategies, combined with chemotherapy or biological therapy, represent a promising future therapeutic avenue for cHL.
Abstract

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