Impact of ART on dynamics of growth factors and cytokines in primary HIV infection

Cytokine. 2020 Jan:125:154839. doi: 10.1016/j.cyto.2019.154839. Epub 2019 Sep 19.

Abstract

Antiretroviral treatment (ART) of Primary HIV Infection (PHI) has demonstrated virological and immunological benefits. The effect of early ART during PHI on the level of growth factors and chemokines modulating immune cell functions remains to be established. The aim of our work was to analyze the dynamics of 27 cytokines, chemokines and growth/regulation factors in plasma of HIV infected patients treated during PHI. Patients with PHI (n = 43) were enrolled before, 24 and 48 weeks after therapy initiation. Quantification of soluble immune mediators was performed in plasma from HIV infected patients and healthy donors (HD, n = 7) by Luminex technology. The cytokines profile was strongly perturbed in primary HIV infected patients when compared to healthy donors (HD). After 48 weeks of ART, some of these factors were restored to HD level (IL-2, IL-5, IL-7, IL-9, IL12p70, TNFα) while others persisted higher than HD (IL-6, IL-10, IL-13). Interestingly, a subset of chemokines, such as IL-8, MCP-1, RANTES and CCL27, and growth factors such as HGF, SCF and GM-CSF, increased during ART, reaching values significantly higher than HD after 48 weeks. Moreover, the G-CSF and MIP-1β soluble mediators were persistently altered and showed an inverse correlation with the CD4/CD8 T cell ratio. The increase of chemokines with antiviral activity and of growth factors with hematopoietic and immunomodulatory properties may have beneficial effects. Other studies are mandatory to evaluate the effects of long lasting levels of these factors to clarify their possible role in the context of protection/pathogenesis.

Keywords: Cytokines profile; Early ART; Growth factors; Primary HIV infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Retroviral Agents / therapeutic use*
  • Antiretroviral Therapy, Highly Active
  • CD4-Positive T-Lymphocytes / cytology
  • CD4-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / immunology
  • Chemokine CCL2 / blood
  • Chemokine CCL27 / blood
  • Chemokine CCL5 / blood
  • Chemokines / blood*
  • Cytokines / blood*
  • Down-Regulation
  • Granulocyte Colony-Stimulating Factor / blood
  • Granulocyte-Macrophage Colony-Stimulating Factor / blood
  • HIV Infections / blood*
  • HIV Infections / drug therapy*
  • Hepatocyte Growth Factor / blood
  • Humans
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Interleukin-10 / blood
  • Interleukin-12 / blood
  • Interleukin-13 / blood
  • Interleukin-2 / blood
  • Interleukin-5 / blood
  • Interleukin-7 / blood
  • Interleukin-8 / blood
  • Principal Component Analysis
  • Stem Cell Factor / blood
  • Tumor Necrosis Factor-alpha / blood

Substances

  • Anti-Retroviral Agents
  • CCL2 protein, human
  • CCL27 protein, human
  • CCL5 protein, human
  • CSF2 protein, human
  • CXCL8 protein, human
  • Chemokine CCL2
  • Chemokine CCL27
  • Chemokine CCL5
  • Chemokines
  • Cytokines
  • HGF protein, human
  • IL2 protein, human
  • IL5 protein, human
  • IL7 protein, human
  • Intercellular Signaling Peptides and Proteins
  • Interleukin-13
  • Interleukin-2
  • Interleukin-5
  • Interleukin-7
  • Interleukin-8
  • KITLG protein, human
  • Stem Cell Factor
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Granulocyte Colony-Stimulating Factor
  • Interleukin-12
  • Hepatocyte Growth Factor
  • Granulocyte-Macrophage Colony-Stimulating Factor