Juan Manuel Carreno Quiroz

Assistant Professor

Icahn School of Medicine at Mount Sinai

United States

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Juan Manuel Carreno Quiroz is an Assistant Professor at the Icahn School of Medicine at Mount Sinai, USA. His research focuses on vaccine responses and immunity related to SARS-CoV-2 and influenza viruses, as demonstrated in his recent publications. He has contributed to studies examining the effects of live-attenuated vaccines, neutralization capabilities across variants, and the implications of vaccination in various patient populations.

Articles (16)

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2025

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2021

Collaborators (12)

David Gerber

Professor of Internal Medicine (Hematology-Oncology) and Clinical Sciences

University of Texas Southwestern Medical Center

UNITED STATES

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Jesse Bloom

Fred Hutchinson Cancer Research Center

UNITED STATES

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Wooseob Kim

Assistant professor

Yonsei University College of Medicine

SOUTH KOREA

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Irene González-Domínguez

UNITED STATES

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Bart L. Haagmans

Principal Investigator / Associate Professor - PhD

Erasmus MC

NETHERLANDS

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Kenneth Matreyek

Assistant Professor

Case Western Reserve University

UNITED STATES

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Jennifer King

Chief Science Officer

UNITED STATES

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Jorge Gomez

Mount Sinai Hospital

UNITED STATES

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Ana Gonzalez-Reiche

Assistant Professor

Icahn School of Medicine at Mount Sinai

UNITED STATES

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Chih-Yuan Hsu

Research Assistant Professor

Vanderbilt University Medical Center

UNITED STATES

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Adolfo Garcia-Sastre

Professor

Icahn School of Medicine at Mount Sinai

UNITED STATES

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Goran Bajic

Assistant Professor

Icahn School of Medicine at Mount Sinai

UNITED STATES

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Juan Manuel Carreno Quiroz

Research Interests

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Articles (16)

Induction of hemagglutinin stalk reactive antibodies by administration of a live-attenuated influenza virus vaccine to children

XBB.1.5 monovalent vaccine induces lasting cross-reactive responses to SARS-CoV-2 variants such as HV.1 and JN.1, as well as SARS-CoV-1, but elicits limited XBB.1.5 specific antibodies

Time-Dependent Effects of Clinical Interventions on SARS-CoV-2 Immunity in Patients with Lung Cancer

Comparative analysis of SARS-CoV-2 neutralization titers reveals consistency between human and animal model serum and across assays

Chronic False Positive Rapid Plasma Reagin (RPR) Tests Induced by COVID-19 Vaccination

An inactivated NDV-HXP-S COVID-19 vaccine elicits a higher proportion of neutralizing antibodies in humans than mRNA vaccination.

Interim safety and immunogenicity results from an NDV-based COVID-19 vaccine phase I trial in Mexico

Receptor-Binding Domain (RBD) Antibodies Contribute More to SARS-CoV-2 Neutralization When Target Cells Express High Levels of ACE2

Reduced antibody activity against SARS-CoV-2 B.1.617.2 delta virus in serum of mRNA-vaccinated individuals receiving tumor necrosis factor-α inhibitors

Activity of convalescent and vaccine serum against SARS-CoV-2 Omicron.

Safety and Immunogenicity Analysis of a Newcastle Disease Virus (NDV-HXP-S) Expressing the Spike Protein of SARS-CoV-2 in Sprague Dawley Rats.

Evidence for retained spike-binding and neutralizing activity against emerging SARS-CoV-2 variants in serum of COVID-19 mRNA vaccine recipients.

Safety and Immunogenicity of a Newcastle Disease Virus Vector-Based SARS-CoV-2 Vaccine Candidate, AVX/COVID-12-HEXAPRO (Patria), in Pigs.

Household level SARS-CoV-2 sero-epidemiology in a high prevalence group of adults and children-implications for community infection control.

Longitudinal analysis of severe acute respiratory syndrome coronavirus 2 seroprevalence using multiple serology platforms.

Introduction of Cysteines in the Stalk Domain of Recombinant Influenza Virus N1 Neuraminidase Enhances Protein Stability and Immunogenicity in Mice

Collaborators (12)

David Gerber

Jesse Bloom

Wooseob Kim

Irene González-Domínguez

Bart L. Haagmans

Kenneth Matreyek

Jennifer King

Jorge Gomez

Ana Gonzalez-Reiche

Chih-Yuan Hsu

Adolfo Garcia-Sastre

Goran Bajic

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