Author

M. A. Pineda

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· 4 Pathology· 1

Signature Assays, Organisms & Methods

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Organism:mouse· 5 Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Research Focus:host-pathogen & immune response· 2 Assay:bulk RNA-seq· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1

Frequent Co-Authors

A. Tarafdar· 3 shared F. E. Lumb· 3 shared M. M. Harnett· 3 shared W. Harnett· 3 shared A. Khan· 2 shared J. Crowe· 2 shared J. Doonan· 2 shared P. A. Hoskisson· 2 shared

Activity by Year

2018-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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3 shared papersImmunology

A. Tarafdar

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

CD20+ T cells are associated with inflammatory responses in experimental arthritis.

M. A. Pineda, P. Pan, Y. Wang, A. Khan, M. H. Nyirenda

This study identifies CD20+ T cells as inflammatory contributors in murine arthritis, showing their expansion and cytokine production in lymph nodes and joints.

bioRxiv · Oct 12, 2021 · PreprintImmunology

ES-62 suppression of arthritis reflects epigenetic rewiring of synovial fibroblasts to a joint-protective phenotype

M. Corbet, M. A. Pineda, K. Yang, A. Tarafdar, S. McGrath, R. Nakagawa, F. E. Lumb, W. Harnett, M. M. Harnett

This study shows ES-62 induces an epigenetic protective phenotype in synovial fibroblasts by remodelling their DNA methylome, potentially offering new therapeutic strategies for rheumatoid arthritis.

bioRxiv · Oct 8, 2020 · PreprintPathology

Loss of α2-6 sialylation promotes the transformation of synovial fibroblasts into a pro-inflammatory phenotype in Rheumatoid Arthritis.

Y. Wang, A. Khan, A. Antonopoulos, L. Bouche, C. D. Buckley, A. Filer, K. Raza, K. Ping-Li, B. Tolusso, E. Gremese, M. Kurowska-Stolarska, S. Alivernini, A. Dell, S. M. Haslam, M. A. Pineda

This study shows that reduced α2-6 sialylation in synovial fibroblasts contributes to a pro-inflammatory phenotype in RA by altering glycosylation pathways.

bioRxiv · Mar 8, 2020Immunology

Parasitic worm-derived ES-62 promotes health- and life-span in high calorie diet-fed mice

J. Crowe, F. E. Lumb, J. Doonan, M. Broussard, A. Tarafdar, M. A. Pineda, C. Landabaso, L. Mulvey, P. A. Hoskisson, S. Babayan, C. Selman, W. Harnett, M. M. Harnett

ES-62, a parasitic worm-derived immunomodulator, improves healthspan and extends lifespan in male mice fed a high-calorie diet.

bioRxiv · Jun 22, 2019 · PreprintImmunology

The parasitic worm product ES-62 normalises the gut microbiota/bone marrow axis in inflammatory arthritis

J. Doonan, A. Tarafdar, M. A. Pineda, F. E. Lumb, J. Crowe, A. M. Khan, P. A. Hoskisson, M. M. Harnett, W. Harnett

This study shows that the parasitic worm product ES-62 reduces joint inflammation in arthritis by normalising gut microbiota and preserving intestinal barrier integrity without requiring live helminth infection.

bioRxiv · Nov 2, 2018Immunology