Author

K. M. McAndrews

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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Biochemistry· 1 Cancer Biology· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Research Focus:host-pathogen & immune response· 3 Approach:experimental assay· 2 Organism:mouse· 2 Assay:proteomics· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1

Frequent Co-Authors

R. Kalluri· 3 shared B. Li· 2 shared H. Sugimoto· 2 shared K. K. Mahadevan· 2 shared S. Shalapour· 2 shared X. Luo· 2 shared A. M. Dyevoich· 1 shared A. M. Sockwell· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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3 shared papersImmunology

R. Kalluri

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Development of an engineered extracellular vesicles-based vaccine platform for combined delivery of mRNA and protein to induce functional immunity

X. Luo, K. M. McAndrews, K. A. Arian, S. J. Morse, V. Boeker, S. V. Kumbhar, Y. Hu, K. K. Mahadevan, K. A. Church, S. Chitta, N. T. Ryujin, J. Hensel, J. Dai, D. P. Dowlatshahi, H. Sugimoto, , R. Kalluri

This paper develops an engineered extracellular vesicles-based vaccine platform for combined mRNA and protein delivery, showing tumor regression and immune responses in preclinical models.

bioRxiv · Mar 14, 2024Immunology

Antigen-presenting type-I conventional dendritic cells facilitate curative checkpoint blockade immunotherapy in pancreatic cancer

K. K. Mahadevan, A. M. Dyevoich, Y. Chen, B. Li, H. Sugimoto, A. M. Sockwell, K. M. McAndrews, H. Wang, S. Shalapour, S. S. Watowich, R. Kalluri

The paper shows that type-I conventional dendritic cells enhance checkpoint blockade immunotherapy effectiveness in pancreatic cancer when combined with pancreatitis.

bioRxiv · Mar 5, 2023 · PreprintCancer Biology

Mutations in the spike RBD of SARS-CoV-2 omicron variant may increase infectivity without dramatically altering the efficacy of current multi-dosage vaccinations

B. Li, X. Luo, K. M. McAndrews, R. Kalluri

The paper analyzes mutations in the SARS-CoV-2 omicron spike RBD, finding increased hydrophilic regions that may enhance infectivity but suggest that multi-dose vaccines can still provide protection against severe disease.

bioRxiv · Dec 8, 2021 · PreprintBiochemistry