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P-2346. Mpox-Specific Cellular and Humoral immunity in Mpox-Survivors Living With HIV

Title: P-2346. Mpox-Specific Cellular and Humoral immunity in Mpox-Survivors Living With HIV
Authors: Stampfer, Samuel D; Sambyal, Shainy; Gangadhara, Sailaja; Kelley, Colleen F; Amara, Rama R; Sheth, Anandi N
Source: Open Forum Infectious Diseases ; volume 12, issue Supplement_1 ; ISSN 2328-8957
Publisher Information: Oxford University Press (OUP)
Publication Year: 2025
Description: Background Mpox is an orthopoxvirus with a rodent reservoir that causes a disease similar to mild smallpox. In 2022, a sexually-transmitted global mpox outbreak infected over 90,000 individuals. Some immunocompromised patients experienced prolonged, severe mpox resulting in significant morbidity, amputations, and death. People living with HIV (PLWH) were at particularly high risk due to impaired cell-mediated immunity, as CD4 and CD8 T-cells help eradicate the virus from infected lesions. Mpox virion total binding titer in PLWH with or without history of mpox infection Methods We compared immune responses to mpox in PLWH who were either mpox-naïve (n = 10) versus mpox-survivors (n = 15). We measured total mpox antibody levels with a novel ELISA assay using lysed mpox virions. We characterized mpox and orthopoxvirus-specific cell-mediated immunity using intracellular cytokine staining with an enhanced protocol to allow detection of low-frequency cellular populations. Poxvirus-specific T-cell responses in PLWH as determined by intracellular cytokine stimulation using live vaccinia virus (MVA), conserved orthopoxvirus peptide pools (VCD4 and VCD8), and mpox-specific peptide pools (MCD4 and MCD8). Pools provided by Alba Grifoni and Alessandro Sette (La Jolla Institute). Interferon-gamma (IFNγ), tumor necrosis factor alpha (TNFα), and interleukin 2 (IL-2) were the predominant cytokines detected. Responders defined as having any CD4 or CD8 response for any of the 9 stimulations above the 90th percentile of the control group. Results Our assays differentiated well between the mpox-naïve and mpox-survivors. All mpox-survivors had binding titers of 10 to 1,000 times background with no antibodies detected in mpox-uninfected PLWH. Mpox-specific CD4 and CD8 responses of 0.01 to 0.3% were present in all infected individuals, comparable to immunocompetent mpox-survivors. The magnitude of mpox-specific T-cell responses correlated well with vaccinia-specific T-cell responses, demonstrating induction of broad ...
Document Type: article in journal/newspaper
Language: English
DOI: 10.1093/ofid/ofae631.2498
Availability: https://doi.org/10.1093/ofid/ofae631.2498; https://academic.oup.com/ofid/article-pdf/12/Supplement_1/ofae631.2498/61676173/ofae631.2498.pdf
Rights: https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.95BF853
Database: BASE