Mariia V. Guryleva

ORCID: 0009-0004-6370-7510
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About
Contact & Profiles
Research Areas
  • HIV Research and Treatment
  • Immunotherapy and Immune Responses
  • T-cell and B-cell Immunology
  • Immune Cell Function and Interaction
  • SARS-CoV-2 and COVID-19 Research
  • Animal Virus Infections Studies
  • vaccines and immunoinformatics approaches
  • Diabetes and associated disorders
  • IL-33, ST2, and ILC Pathways

Karolinska Institutet
2020-2025

University Medical Center Utrecht
2024

Lomonosov Moscow State University
2020

HIV broadly neutralizing antibodies (bnAbs) can suppress viremia and protect against infection. However, their elicitation is made difficult by low frequencies of appropriate precursor B cell receptors the complex maturation pathways required to generate bnAbs from these precursors. Antibody genes be engineered into cells for expression as both a functional antigen receptor on surfaces secreted antibody. Here, we show that bnAb-engineered primary mouse adoptively transferred vaccinated in...

10.1038/s41467-020-19650-8 article EN cc-by Nature Communications 2020-11-17

HIV broadly neutralizing antibodies (bnAbs) can suppress viremia and protect against infection 1 . However, their elicitation is made difficult by low frequencies of appropriate precursor B cell receptors the complex maturation pathways required to generate bnAbs from these precursors 2 Antibody genes be engineered into cells for expression as both a functional receptor on surfaces secreted antibody 3–5 Here, we show that bnAb-engineered primary mouse adoptively transferred vaccinated in...

10.1101/2020.03.17.989699 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2020-03-17

<title>Abstract</title> The continued evolution of SARS-CoV-2 underscores the need to understand qualitative aspects humoral immune response elicited by spike immunization. Here, we combined monoclonal antibody (mAb) isolation with deep B cell receptor (BCR) repertoire sequencing rhesus macaques immunized prefusion-stabilized glycoprotein. Longitudinal tracing spike-sorted lineages in multiple compartments demonstrated increasing somatic hypermutation and broad dissemination vaccine-elicited...

10.21203/rs.3.rs-3958951/v1 preprint EN cc-by Research Square (Research Square) 2024-02-26

Abstract Objectives The caecum bridges the small and large intestine plays a front‐line role in discriminating gastrointestinal antigens. Although dysregulated acute chronic conditions, tissue is often overlooked immunologically. Methods To address this issue, we applied single‐cell transcriptomic‐V(D)J sequencing to FACS‐isolated CD45 + caecal patch/lamina propria leukocytes from healthy (5‐year‐old) female rhesus macaque ex vivo coupled these data VDJ deep reads haematopoietic tissues....

10.1002/cti2.1508 article EN cc-by Clinical & Translational Immunology 2024-01-01

Abstract The continued evolution of SARS-CoV-2 underscores the need to understand qualitative aspects humoral immune response elicited by spike immunization. Here, we combine monoclonal antibody (mAb) isolation with deep B cell receptor (BCR) repertoire sequencing rhesus macaques immunized prefusion-stabilized glycoprotein. Longitudinal tracing spike-sorted lineages in multiple compartments demonstrates increasing somatic hypermutation and broad dissemination vaccine-elicited cells draining...

10.1038/s41467-024-50286-0 article EN cc-by Nature Communications 2024-07-27

Summary Protective antibodies against HIV-1 require unusually high levels of somatic hypermutations (SHMs) introduced in germinal centers (GCs). To achieve this, a sequential vaccination approach was proposed. Using antibody knock-in mice with fate-mapping genes, we examined if antigen affinity affects the outcome B cell recall response. Compared to boost, low boost resulted decreased numbers memory-derived cells secondary GCs, but higher average SHM, indicating an threshold for memory enter...

10.1101/2024.04.19.590239 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-04-23
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