Author

B. B. Andrade

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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Approach:experimental assay· 4 Research Focus:host-pathogen & immune response· 4 Assay:bulk RNA-seq· 2 Organism:human· 2 Organism:mouse· 2 Organism:rat· 2 Research Focus:differential expression· 1 Approach:statistical model· 1

Frequent Co-Authors

D. L. Barber· 4 shared C. L. Vinhaes· 3 shared K. D. Kauffman· 3 shared K. D. Mayer-Barber· 3 shared L. E. Via· 3 shared P. J. Baker· 3 shared A. C. Bohrer· 2 shared A. Sette· 2 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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4 shared papersImmunology

D. L. Barber

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5 papers

Recent·Most cited

The inflammatory microenvironment of the lung at the time of infection governs innate control of SARS-CoV-2 replication

P. J. Baker, A. C. Bohrer, E. Castro, E. P. Amaral, M. Snow-Smith, F. Torres-Juarez, S. T. Gould, A. T. Queiroz, E. R. Fukutani, C. M. Jordan, J. S. Khillan, K. Cho, D. L. Barber, B. B. Andrade, R. F. Johnson, , K. D. Mayer-Barber

This study shows that pre-existing lung inflammation reduces SARS-CoV-2 replication by activating innate immune pathways, highlighting the role of the inflammatory microenvironment in controlling viral infection.

bioRxiv · Mar 27, 2024Immunology

CD4 T cells are rapidly depleted from tuberculosis granulomas following acute SIV co-infection

T. W. Foreman, C. E. Nelson, K. D. Kauffman, N. E. Lora, C. L. Vinhaes, D. E. Dorosky, S. W. Sakai, F. Gomez, J. D. Fleegle, M. Parham, S. R. Perera, C. S. Lindestam Arlehamn, A. Sette, Tuberculosis Imaging Program, J. M. Brenchley, , D. L. Barber

This study shows that acute SIV co-infection rapidly depletes CD4 T cells from tuberculosis granulomas before systemic CD4 T cell loss or disease reactivation.

bioRxiv · Dec 17, 2021Immunology

Eosinophils are an integral component of the pulmonary granulocyte response in Tuberculosis and promote host resistance in mice

A. C. Bohrer, E. Castro, Z. Hu, A. T. L. Queiroz, C. E. Tocheny, M. Assmann, S. Sakai, C. Nelson, P. J. Baker, H. Ma, L. Wang, W. Zilu, E. du Bruyn, C. Riou, K. D. Kauffman, , K. D. Mayer-Barber

This study shows eosinophils are recruited to tuberculosis-infected lung tissue in mice and contribute to host resistance against Mtb infection.

bioRxiv · May 29, 2021Immunology

PD-1 blockade exacerbates Mycobacterium tuberculosis infection in rhesus macaques

K. D. Kauffman, S. Sakai, N. E. Lora, S. Namasivayam, P. J. Baker, O. Kamenyeva, T. W. Foreman, C. E. Nelson, D. Oliveira-de-Souza, C. L. Vinhaes, Z. Yaniv, C. S. Lindestam Arleham, A. Sette, G. J. Freeman, R. Moore, , D. L. Barber

This study shows that PD-1 blockade worsens Mycobacterium tuberculosis infection in rhesus macaques by increasing bacterial loads and altering immune responses.

bioRxiv · Aug 5, 2020Immunology

Aging increases the systemic molecular degree of inflammatory perturbation in patients with tuberculosis

D. Oliveira-de-Souza, C. L. Vinhaes, M. B. Arriaga, N. Pavan Kumar, A. T. L. Queiroz, K. F. Fukutani, S. Babu, B. B. Andrade

This study finds that aging increases the molecular degree of inflammatory perturbation in tuberculosis patients, with higher values observed in adults compared to children.

bioRxiv · Mar 10, 2020Immunology