Title
Cytokine expression in Treponema pallidum infection
Date Issued
11 June 2019
Access level
open access
Resource Type
journal article
Author(s)
Kojima N.
Siebert J.C.
Maecker H.
Rosenberg-Hasson Y.
Leon S.R.
Klausner J.D.
Publisher(s)
BioMed Central Ltd.
Abstract
Background: Current syphilis tests cannot distinguish between active and past syphilis among patients with serofast rapid plasma reagin (RPR) titers. We investigated whether cytokine profiles might provide insight in the differentiation of active and treated syphilis. Methods: We collected quarterly serum samples from participants at risk for incident syphilis in a prospective cohort study of men and male-to-female transgender women. We defined incident syphilis as a new RPR titer ≥ 1:8 or a fourfold increase from a prior RPR titer and a positive Treponema pallidum particle agglutination assay. We measured cytokine expression using a 63-multiplex bead-based Luminex assay (eBiosciences/Affymetrix, San Diego, California, USA). We used tertile bins and Chi square tests to identify differences in proportions of cytokines between samples from patients with active and treated syphilis. We constructed a network of cytokine profiles from those findings. We used R software (R version 3.4.1, R, Vienna, Austria) to fit models. Results: We identified 20 pairs of cytokines (out of 1953 possible pairs) that differed between active and treated syphilis. From those, we identified three cytokine networks of interest: an Eotaxin-Rantes-Leptin network, a Mig-IL1ra-Trail-CD40L network, and an IL12p40-IL12p70 network. Conclusions: Differences in cytokine profiles are present among men and male-to-female transgender women with active and treated syphilis. Cytokine assays may be a potentially useful tool for identifying active syphilis among patients with serologic syphilis reactivity.
Volume
17
Issue
1
Language
English
OCDE Knowledge area
Medicina general, Medicina interna
Enfermedades infecciosas
Subjects
Scopus EID
2-s2.0-85067260226
PubMed ID
Source
Journal of Translational Medicine
ISSN of the container
1479-5876
Sponsor(s)
This study was funded by the National Institute of Allergy and Infectious Diseases (1R01AI099727 and 1R01AI139265). JDK acknowledges funding from NIH P30MH058107 (The Center for HIV Identification, Prevention, and Treat‑ ment Services) and NIH/NIAID AI028697 (UCLA Center for AIDS Research).
The authors want to acknowledge the staff and patients at Epicentro and the Barton Health Center for hosting and participating in the study in Lima, Peru. We also thank Justin Sonnenburg, Christopher Gardner, and Gabi Fragiadakis for sharing healthy control data from their diet modification study. NK is sup‑ ported by the Fogarty International Center of the National Institutes of Health (NIH) under Award Number D43TW009343 and the University of California Global Health Institute (UCGHI). The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH or UCGHI.
Sources of information:
Directorio de Producción Científica
Scopus