Chemokine profile in the serum of patients with leptospirosis

Front Cell Infect Microbiol. 2024 Oct 29:14:1484291. doi: 10.3389/fcimb.2024.1484291. eCollection 2024.

Abstract

Introduction: Leptospirosis is a global zoonosis that affects more than one million people per year, with a lethality rate of approximately 15%. Chemokines are crucial in the immune response against Leptospira, recruiting leukocytes to the site of infection and regulating immune activity. In previous studies, we have shown that CCL2, CXCL5, and CCL8 are involved in the leptospirosis process, although the mechanisms are not understood.

Methods: In this study, we present the frequency of Leptospira serovars in human samples. We then evaluated the profile of various chemokines in sera from patients diagnosed with leptospirosis, assessing the possible correlation between them. Moreover, we evaluated the changes in the chemokine profile on different days after the first symptoms. The frequency of the Leptospira serovars in human samples is presented.

Results and discussion: The main findings were that CCL5, CXCL5, and CXCL9 are highly expressed during leptospirosis, indicating a special role of these molecules in the immunity and pathogenesis of the disease. The correlation analysis of detected chemokines CXCL11, CXCL9, CCL3, and CCL2 helps to clarify the role of each cytokine in leptospirosis. The possible use of CCL5 as a biomarker for complementary diagnosis of the disease is suggested.

Keywords: Copenhageni serovar; Leptospira; chemokines; diagnosis; leptospirosis; protein interaction.

MeSH terms

  • Adult
  • Biomarkers / blood
  • Chemokine CCL2 / blood
  • Chemokine CCL3 / blood
  • Chemokine CCL5 / blood
  • Chemokine CXCL11 / blood
  • Chemokine CXCL9 / blood
  • Chemokines* / blood
  • Female
  • Humans
  • Leptospira* / immunology
  • Leptospirosis* / blood
  • Leptospirosis* / immunology
  • Male
  • Serogroup

Substances

  • Chemokines
  • Chemokine CCL5
  • Chemokine CXCL9
  • Biomarkers
  • CCL5 protein, human
  • CXCL9 protein, human
  • Chemokine CCL2
  • Chemokine CCL3
  • Chemokine CXCL11
  • CXCL11 protein, human
  • CCL3 protein, human

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work received grants from Fundação de Amparo à Pesquisa do Estado de São Paulo - FAPESP (2017/20903-6) and Fundação Butantan (001/0708/000.200/2024). IHMM, CES, and GSF received scholarships from Instituto Butantan - Secretaria da Saúde do Estado de São Paulo. The funders had no role in the study design, data collection and analysis, writing of the manuscript, or decision to publish it.