Meegan R. Anderson
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Meegan R. Anderson has a total of 40 co-authors. Here are the top co-authors by number of shared publications:
- Mariluz Araínga
New Iberia Research Center, University of Louisiana at Lafayette, New Iberia, Louisiana, USA
2 shared publications - Michael D. McRaven
Affiliation Department of Cell and Developmental Biology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States of America
2 shared publications - Ramon Lorenzo-Redondo
Division of Infectious Diseases, Feinberg School of Medicine, Northwestern University, United States
2 shared publications - Thomas J. Hope
Department of Cell and Developmental Biology, Feinberg School of Medicine, Northwestern University, United States
2 shared publications - Yanique Thomas
Affiliation Department of Cell and Developmental Biology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States of America
2 shared publications - Ann M. Carias
Department of Cell and Developmental Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA
1 shared publication
Latest Publications
- 6 November 2024
- Published by SAGE Publications in AIDS Research and Human Retroviruses
- Vol. 40 (11) , 637-648
PET/CT Targeted Tissue Sampling Reveals Intravenously Administered HGN194 IgG1 Affects HIV Distribution after Rectal Exposure
Neutralizing monoclonal antibodies hold great potential for prevention of human immunodeficiency virus (HIV) acquisition. IgG is the most abundant antibody in human serum, has a long half-life, and potent effector functions, making it a prime candidate for an HIV prevention therapeutic. We combined Positron Emission Tomography imaging and fluorescent microscopy of 64 Cu-labeled, photoactivatable-green fluorescent protein HIV (PA-GFP-BaL) and fluorescently labeled HGN194 IgG1 to determine whether intravenously instilled IgG influences viral interaction with mucosal barriers and viral penetration in colorectal tissue 2 h after rectal viral challenge. Our results show that IgG1 did not alter the number of virions found throughout the colon or viral penetration into the epithelium of the rectum or descending colon. A minor increase in virions was observed in the transverse colon of IgG1 treated animals. Overall, the number of viral particles found in the mesenteric lymph nodes was low. However, IgG1 administration resulted in a significant reduction of virions found in mesenteric lymph nodes. Taken together, our results show that HGN194 IgG1 does not prevent virions from penetrating into the colorectal mucosa but may perturb HIV virion access to the lymphatic system.
- 6 November 2024
- Published by SAGE Publications in AIDS Research and Human Retroviruses
- Vol. 40 (11) , 637-648
PET/CT Targeted Tissue Sampling Reveals Intravenously Administered HGN194 IgG1 Affects HIV Distribution after Rectal Exposure
Neutralizing monoclonal antibodies hold great potential for prevention of human immunodeficiency virus (HIV) acquisition. IgG is the most abundant antibody in human serum, has a long half-life, and potent effector functions, making it a prime candidate for an HIV prevention therapeutic. We combined Positron Emission Tomography imaging and fluorescent microscopy of 64 Cu-labeled, photoactivatable-green fluorescent protein HIV (PA-GFP-BaL) and fluorescently labeled HGN194 IgG1 to determine whether intravenously instilled IgG influences viral interaction with mucosal barriers and viral penetration in colorectal tissue 2 h after rectal viral challenge. Our results show that IgG1 did not alter the number of virions found throughout the colon or viral penetration into the epithelium of the rectum or descending colon. A minor increase in virions was observed in the transverse colon of IgG1 treated animals. Overall, the number of viral particles found in the mesenteric lymph nodes was low. However, IgG1 administration resulted in a significant reduction of virions found in mesenteric lymph nodes. Taken together, our results show that HGN194 IgG1 does not prevent virions from penetrating into the colorectal mucosa but may perturb HIV virion access to the lymphatic system.
- 22 November 2023
- Published by American Society for Clinical Investigation in JCI Insight
- Vol. 8 (22)
Blockade of TGF-β signaling reactivates HIV-1/SIV reservoirs and immune responses in vivo
- 22 November 2023
- Published by American Society for Clinical Investigation in JCI Insight
- Vol. 8 (22)
Blockade of TGF-β signaling reactivates HIV-1/SIV reservoirs and immune responses in vivo