dc.contributor.author
Moraes-Cardoso, Igor
dc.contributor.author
Benet, Susana
dc.contributor.author
Carabelli, Julieta
dc.contributor.author
Perez-Zsolt, Daniel
dc.contributor.author
Mendoza, Adrià
dc.contributor.author
Rivero, Ángel
dc.contributor.author
Alemany, Andrea
dc.contributor.author
Descalzo Jorro, Vicente
dc.contributor.author
Alarcón-Soto, Yovaninna
dc.contributor.author
Grifoni, Alba
dc.contributor.author
Sette, Alessandro
dc.contributor.author
Moltó, José
dc.contributor.author
Marc, Aurélien
dc.contributor.author
Marks, Michael
dc.contributor.author
Mitjà, Oriol
dc.contributor.author
Brander, Christian
dc.contributor.author
Paredes, Roger
dc.contributor.author
Izquierdo Useros, Nuria
dc.contributor.author
Carrillo, Jorge
dc.contributor.author
Suñer, Clara
dc.contributor.author
Olvera, Alex
dc.contributor.author
Mothe, Beatriz
dc.contributor.author
Bailón, Lucía
dc.contributor.author
Sabato, Sofía
dc.contributor.author
Torrano, Pamela
dc.contributor.author
Ubals, María
dc.contributor.author
Boreika, Rytis
dc.contributor.author
Gallemí, Marçal
dc.contributor.author
Molina-Molina, Elisa
dc.contributor.author
Muñoz-Basagoiti, Jordana
dc.contributor.author
Raïch-Regué, Dàlia
dc.contributor.author
Coll, Pep
dc.contributor.author
Fernández Pérez, Javier
dc.contributor.author
Pérez, Félix
dc.contributor.author
Reguant, Joan
dc.contributor.author
Arando, Maider
dc.contributor.author
Néstor Garcia, Jorge
dc.contributor.author
Monforte, Arnau
dc.contributor.author
Álvarez, Patricia
dc.contributor.author
Guedj, Jeremie INSERM (París)
dc.contributor.author
Universitat Autònoma de Barcelona
dc.identifier
https://ddd.uab.cat/record/309348
dc.identifier
urn:10.1016/S2666-5247(24)00074-0
dc.identifier
urn:oai:ddd.uab.cat:309348
dc.identifier
urn:scopus_id:85195392768
dc.identifier
urn:articleid:26665247v5n8p100859
dc.identifier
urn:pmid:38857615
dc.identifier
urn:oai:egreta.uab.cat:publications/82d0e95f-c8d6-41d7-bdb6-238559c89e52
dc.description.abstract
Background: Since the emergence of the global mpox outbreak in May, 2022, more than 90 000 cases have been diagnosed across 110 countries, disproportionately affecting people with HIV. The durability of mpox-specific immunity is unclear and reinfections have been reported. We aimed to compare mpox immune responses up to 6 months after diagnosis in participants with and without HIV and assess their effect on disease severity and viral clearance dynamics. Methods: This study was embedded within a prospective, observational, multicentre cohort study of viral clearance dynamics among people with mpox in Spain (MoViE). We included women and men aged 18 years or older, who had signs of mpox, and reported having symptom onset within the previous 10 days at the moment of mpox diagnosis from three sex clinics of the Barcelona metropolitan area. Samples from skin ulcers were collected weekly to estimate the time to clear monkeypox virus (MPXV) from skin lesions. Blood samples were taken at diagnosis, 29, 91, and 182 days later for immune analysis. This included quantifying IgG and IgA against three mpox antigens by ELISA, evaluating in-vitro neutralisation, and characterising mpox-specific T-cell responses using interferon γ detecting enzyme-linked immunospot (ELISpot) assay and multiparametric flow cytometry. Findings: Of the 77 originally enrolled participants, we included 33 participants recruited between July 19, and Oct 6, 2022. Participants without HIV (19 [58%] participants) and participants with HIV (14 [42%] participants) had similar clinical severity and time to MPXV clearance in skin lesions. Participants with HIV had a CD4 T-cell count median of 777 cells per μL (IQR 484-1533), and 11 (78%) of 14 were virally suppressed on antiretroviral therapy. Nine (27%) of 33 participants were age 49 years or older. 15 (45%) of 33 participants were originally from Spain, and all participants were men. Early humoral responses, particularly concentrations and breadth of IgG and IgA, were associated with milder disease and faster viral clearance. Orthopoxvirus-specific T cells count was also positively correlated with MPXV clearance. Antibody titres declined more rapidly in participants with HIV, but T-cell responses against MPXV were sustained up to day 182 after diagnosis, regardless of HIV status. Interpretation: Higher breadth and magnitude of B-cell and T-cell responses are important in facilitating local viral clearance, limiting mpox dissemination, and reducing disease severity in individuals with preserved immune system. Antibodies appear to contribute to early viral control and T-cell responses are sustained over time, which might contribute to milder presentations during reinfection. Funding: Fundació Lluita contra les Infeccions, IrsiCaixa, and Consorcio Centro de Investigación Biomédica en Red, Instituto de Salud Carlos III, Ministerio de Ciencia, Innovación e Universidades.
dc.format
application/pdf
dc.relation
Agencia Estatal de Investigación PID2020-117145RB-I00
dc.relation
The Lancet microbe ; Vol. 5 Núm. 8 (august 2024), p. 100859
dc.rights
Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original.
dc.rights
https://creativecommons.org/licenses/by-nc/4.0/
dc.title
Immune responses associated with mpox viral clearance in men with and without HIV in Spain : a multisite, observational, prospective cohort study