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Characterization of Vaccine-induced Responses Against Monkeypox (MoVIHvax) An Observational Prospective Cohort Study

Characterization of Vaccine-induced Responses Against Monkeypox (MoVIHvax) An Observational Prospective Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05562323
Enrollment
100
Registered
2022-09-30
Start date
2022-09-14
Completion date
2026-08-01
Last updated
2026-07-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Monkeypox

Keywords

Monkeypox vaccine, Immune responses, HIV

Brief summary

This observational study has been designed to characterize humoral and cellular immune responses after vaccination against monkeypox (MKP) in HIV positive and negative individuals at high risk of MKP infection during the vaccination campaign in the current monkeypox outbreak.

Detailed description

Of the 23,837 cases of monkeypox reported in the European Region of the WHO, 7.037 have been identified in Spain, according to the National Epidemiological Surveillance Network (RENAVE). Most of diagnosed individuals are men born in Spain, being nearly 40% HIV positive. The clinical evolution was satisfactory, although 3-7% of cases required hospitalization. Given the limited number of available doses of the MVA-BN vaccine, it has been recently approved its use as a single intradermal dose. However, this posology can be more reactogenic than subcutaneous injection and there is limited data on its immunogenicity and effectiveness in people living with HIV (PLWH), which account for about half of the monkeypox cases in the current outbreak. The present observational study has been designed to investigate the humoral and cellular immune responses following monkeypox vaccination in PLWH.

Interventions

None listed

Sponsors

Fundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia
Lead SponsorOTHER
IrsiCaixa
CollaboratorOTHER
BCN Checkpoint
CollaboratorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

1. Adult individuals of ≥18 years old. 2. Willing to comply with the requirements of the protocol and available for follow-up for the planned duration of the trial. 3. Has understood the information provided and capable of giving informed consent.

Exclusion criteria

1\. Participant has any medical condition and/or finding that in the investigator opinion might increase participant risks, interfere with the study or impair interpretation of study data.

Design outcomes

Primary

MeasureTime frameDescription
Proportion of participants with detectable anti-orthopox antibodiesBetween day 29 - 90Proportion of participants with detectable anti-orthopox antibodies at 29 - 90 days following first MVA-BN vaccination
Quantification of anti-orthopox antibodiesBetween day 29 - 90Quantification of anti-orthopox antibodies at 29 - 90 days following first MVA-BN vaccination

Secondary

MeasureTime frameDescription
Changes of the immunogenicity after the first vaccine doseBetween day 29 - 90 and between 150-180 (after the first dose) and between 29 - 90 and between 150-180 (after the second dose if applicable)The geometric mean fold rise (GMFR) in anti-orthopox antibody titers from baseline to Day 29-90 and 150-180 after the first dose of MVA-BN and to 29-90 and 150-180 after the second dose (if applicable)
To compare immunogenicity between HIV negative and HIV positive individualsBetween day 29 - 90 and between 150-180 (after the first dose) and between 29 - 90 and between 150-180 (after the second dose if applicable)To compare the GMFR between HIV negative and HIV positive individuals
Neutralization capacity of anti-orthopox antibodiesBetween day 29 - 90 and between 150-180 (after the first dose) and between 29 - 90 and between 150-180 (after the second dose if applicable)Neutralization titers measured as the reciprocal dilution inhibiting 50% of the infection (ID50) will be reported using a live virus assay (VNA) to measure cytopathic effect in Vero E6 cells after the first dose of MVA-BN.
To compare neutralization capacity between HIV negative and HIV positive individualsBetween day 29 - 90 and between 150-180 (after the first dose) and between 29 - 90 and between 150-180 (after the second dose if applicable)To compare ID50 between HIV negative and HIV positive individuals

Countries

Spain

Contacts

CONTACTBeatriz Mothe, PhD, MD
bmothe@irsicaixa.es676142408
CONTACTSusana Benet, PhD, MD
sbenet@lluita.org676142408

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 8, 2026