Author

H. Mattoo

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Immunology· 5

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 5 Approach:experimental assay· 3 Organism:human· 3 Approach:statistical model· 3 Assay:bulk RNA-seq· 2 Organism:mouse· 2 Assay:ATAC-seq· 1 Research Focus:cell signaling & trafficking· 1

Frequent Co-Authors

G. J. Yuen· 3 shared S. Pillai· 3 shared N. Sun· 2 shared V. Mahajan· 2 shared V. S. Mahajan· 2 shared V. V. Viswanadham· 2 shared A. Viguier· 1 shared C. Annaiah· 1 shared

Activity by Year

2018-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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3 shared papersImmunology

G. J. Yuen

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

GM-CSF-activated human dendritic cells promote type1 T follicular helper cells (Tfh1) polarization in a CD40-dependent manner

S. Korniotis, M. Saichi, C. Trichot, C. Hoffmann, E. Amblard, A. Viguier, S. Grondin, F. Noel, H. Mattoo, V. Soumelis

This study shows GM-CSF-activated human dendritic cells drive Tfh1 differentiation via CD40-dependent mechanisms, with implications for infections like tuberculosis and COVID-19.

bioRxiv · Apr 28, 2022 · PreprintImmunology

Network-based integration of epigenetic landscapes unveils molecular programs underlying human T follicular helper cell differentiation

V. S. Mahajan, S. A. Rahman, V. V. Viswanadham, G. J. Yuen, N. Sun, H. Mattoo, S. S. Pillai, J. Das

The paper integrates epigenomic data with a protein interactome to identify molecular programs driving human Tfh cell differentiation and links these to immune signaling in severe COVID-19.

bioRxiv · May 19, 2021 · PreprintImmunology

B1 and B2 B cells are characterized by distinct CpG modification states at DNMT3A-maintained enhancers

V. S. Mahajan, H. Mattoo, N. Sun, V. V. Viswanadham, G. J. Yuen, H. Allard-Chamard, M. Ahmad, S. J. H. Murphy, C. Annaiah, Y. Tuncay, S. Pillai

The paper identifies distinct CpG modification states in B1 and B2 B cells at DNMT3A-maintained enhancers, showing differential methylation dynamics during development.

bioRxiv · Apr 30, 2020Immunology

Alterations in sialic-acid O-acetylation glycoforms during murine erythrocyte development

V. Mahajan, F. Alsufyani, H. Mattoo, I. Rosenberg, S. Pillai

This study shows that CASD1 is essential for 9-O-acetylation of sialic acids on erythroid cells in vivo, and that this modification is recognized by specific virolectins and contributes to the TER-119 epitope.

bioRxiv · Nov 14, 2018Immunology

The expansion in lymphoid organs of IL-4+ BATF+ T follicular helper cells is linked to IgG4 class switching in vivo

S. Pillai, J. Stone, S. Nakamura, T. Kiyoshima, J. Daccache, M. Yamauchi, H. Yamamoto, T. Saeki, M. Moriyama, M. Ohta, N. Ishiguro, G. J. Yuen, S. L. Murphy, V. Mahajan, H. Mattoo, T. Maehara

The paper identifies IL-4+ BATF+ T follicular helper cells in IgG4-related disease that correlate with IgG4 class switching in lymphoid organs.

bioRxiv · Mar 19, 2018Immunology