International Journal of Infectious Diseases (May 2020)

A unique immune signature of serum cytokine and chemokine dynamics in patients with Zika virus infection from a tropical region in Southern Mexico

  • Joaquín Zuñiga,
  • José Alberto Choreño-Parra,
  • Luis Jiménez-Alvarez,
  • Alfredo Cruz-Lagunas,
  • José Eduardo Márquez-García,
  • Gustavo Ramírez-Martínez,
  • Aminadab Goodina,
  • Erika Hernández-Montiel,
  • Luis Alejandro Fernández-López,
  • María Fernanda Cabrera-Cornejo,
  • Carlos Cabello,
  • Manuel Castillejos,
  • Andrés Hernández,
  • Nora E. Regino-Zamarripa,
  • Criselda Mendoza-Milla,
  • Héctor Vivanco-Cid,
  • Alejandro Escobar-Gutierrez,
  • Salvador Fonseca-Coronado,
  • Pablo F. Belaunzarán-Zamudio,
  • Santiago Pérez-Patrigeon,
  • Lourdes Guerrero,
  • Justino Regalado,
  • Gabriel Nájera-Cancino,
  • Sandra Caballero-Sosa,
  • Héctor Rincón-León,
  • Mary Smolskis,
  • Allyson Mateja,
  • Sally Hunsberger,
  • John H. Beigel,
  • Guillermo Ruiz-Palacios

Journal volume & issue
Vol. 94
pp. 4 – 11

Abstract

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Objectives: To describe the kinetics of circulating cytokines and chemokines in humans with ZIKAV infection. Methods: Serum levels of different immune mediators in patients with ZIKAV infection were measured at distinct stages of the disease, as well as in culture supernatants from human monocytes infected with a clinical ZIKAV isolate. We also looked for clinical features associated with specific immune signatures among symptomatic patients. Results: We evaluated 23 ZIKAV-infected patients. Their mean age was 32 ± 8.3 years and 65% were female. ZIKAV patients showed elevated IL-9, IL-17A, and CXCL10 levels at acute stages of the disease. At day 28, levels of CCL4 and CCL5 were increased, whereas IL-1RA, CXCL8 and CCL2 were decreased. At baseline, IL-7 was increased among patients with headache, whereas CCL2, and CCL3 were decreased in patients with bleeding and rash, respectively. Our clinical ZIKAV isolate induced a broad immune response in monocytes that did not resemble the signature observed in ZIKAV patients. Conclusions: We showed a unique immune signature in our cohort of ZIKAV-infected patients. Our study may provide valuable evidence helpful to identify immune correlates of protection against ZIKAV.

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