HIV-1 evades virus-specific IgG2 and IgA responses by targeting systemic and intestinal B cells via long-range intercellular conduits

Nanotubular Highways for Intercellular Organelle Transport

Rustom, A., Saffrich, R., Markovic, I., Walther, P., & Gerdes, H.-H. (2004) · Science · doi:10.1126/science.1093133 · Cited by 2,038

Abnormalities of B-Cell Activation and Immunoregulation in Patients with the Acquired Immunodeficiency Syndrome

Lane, H. C., Masur, H., Edgar, L. C., Whalen, G., Rook, A. H., & Fauci, A. S. (1983) · New England Journal of Medicine · doi:10.1056/nejm198308253090803 · Cited by 1,600

Importance of the nef gene for maintenance of high virus loads and for development of AIDS

Kestier, H. W., Ringler, D. J., Mori, K., Panicali, D., Sehgal, P. K., Daniel, M. D., & Desrosiers, R. C. (1991) · Cell · doi:10.1016/0092-8674(91)90097-i · Cited by 1,593

Blimp-1 Orchestrates Plasma Cell Differentiation by Extinguishing the Mature B Cell Gene Expression Program

Shaffer, A. L., Lin, K., Kuo, T. C., Yu, X., Hurt, E. M., Rosenwald, A., Giltnane, J. M., Yang, L., Zhao, H., Calame, K. L., et al. (2002) · Immunity · doi:10.1016/s1074-7613(02)00335-7 · Cited by 1,048

Evidence for HIV-associated B cell exhaustion in a dysfunctional memory B cell compartment in HIV-infected viremic individuals

Moir, S. L., Ho, J., Malaspina, A., Wang, W., DiPoto, A. C., O’Shea, M. A., Roby, G. A., Kottilil, S., Arthos, J. A., Proschan, M. A., et al. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20072683 · Cited by 894

Subcapsular sinus macrophages in lymph nodes clear lymph-borne viruses and present them to antiviral B cells

Junt, T., Moseman, E. A., Iannacone, M., Massberg, S., Lang, P. A., Boes, M., Fink, K., Henrickson, S. E., Shayakhmetov, D. M., Di Paolo, N. C., et al. (2007) · Nature · doi:10.1038/nature06287 · Cited by 846

Transcription factor IRF4 controls plasma cell differentiation and class-switch recombination

Klein, U., Casola, S. S., Cattoretti, G., Shen, Q. “., Lia, M., Mo, T., Ludwig, T. E., Rajewsky, K., & Dalla‐Favera, R. (2006) · Nature Immunology · doi:10.1038/ni1357 · Cited by 820

HIV vaccine design and the neutralizing antibody problem

Burton, D. R., Desrosiers, R. C., Doms, R. W., Koff, W. C., Kwong, P. D., Moore, J. P., Nabel, G. J., Sodroski, J., Wilson, I. A., & Wyatt, R. T. (2004) · Nature Immunology · doi:10.1038/ni0304-233 · Cited by 765

Nonlytic Egress and Transmission in the Virus World

Altan‐Bonnet, N., & Panigrahi, M. (2025) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-052521-120140 · Cited by 11

HIV-1 and the Macrophage

Bol, S. M., Jiménez, V. C., Kootstra, N. A., & Wout, A. B. V. ’. (2011) · Future Virology · doi:10.2217/fvl.10.93 · Cited by 10

The Good, the Bad, and the Ugly of Dendritic Cells during Prion Disease

Mabbott, N. A., & Bradford, B. M. (2015) · Journal of Immunology Research · doi:10.1155/2015/168574 · Cited by 10

Signature molecules expressed differentially in a liver disease stage-specific manner by HIV-1 and HCV co-infection

Whitmill, A., Kim, S., Rojas, V. K., Gulraiz, F., Afreen, K. S., Jain, M. K., Singh, M., & Park, I.-W. (2018) · PLoS ONE · doi:10.1371/journal.pone.0202524 · Cited by 10

Inhibitors of the 5-lipoxygenase arachidonic acid pathway induce ATP release and ATP-dependent organic cation transport in macrophages

Souza, H. A. D. S., de Lira, M. N., Costa‐Junior, H. M., da Cruz, C. M., Vasconcellos, J. S. S., Mendes, A. N., Pimenta-Reis, G., Alvarez, C. L., Faccioli, L. H., Serezani, C. H., et al. (2014) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2014.04.006 · Cited by 10

Persistent subclinical immune defects in HIV-1-infected children treated with antiretroviral therapy

van den Heuvel, D., Driessen, G. J. A., Berkowska, M. A., van der Burg, M., Langerak, A. W., Zhao, D., Charif, H., Hartwig, N. G., van Rossum, A. M. C., Fraaij, P. L. A., et al. (2015) · AIDS · doi:10.1097/qad.0000000000000765 · Cited by 9

Non-muscle myosin heavy chain 9 is a critical factor for infectious pancreatic necrosis virus cellular entry

Shao, L., Zhao, J., & Tang, Q. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.736138 · Cited by 9

A gut triumvirate rules homeostasis

Chorny, A., & Cerutti, A. (2011) · Nature Medicine · doi:10.1038/nm.2592 · Cited by 9

HIV-Specific Antibody Responses in HIV-Infected Patients: From a Monoclonal to a Polyclonal View

Gallerano, D., Cabauatan, C. R., Sibanda, E., & Valenta, R. (2015) · International Archives of Allergy and Immunology · doi:10.1159/000438484 · Cited by 9

Pigs as an experimental model for systemic Mycobacterium avium infectious disease

Hibiya, K., Furugen, M., Higa, F., Tateyama, M., & Fujita, J. (2011) · Comparative Immunology Microbiology and Infectious Diseases · doi:10.1016/j.cimid.2011.09.001 · Cited by 9

Understanding the key functions of Myosins in viral infection

He, J., Qiu, Y., Tan, L., Duan, D., Yuan, X., Yang, L., & Wang, A. (2022) · Biochemical Society Transactions · doi:10.1042/bst20211239 · Cited by 9

Human immunodeficiency virus transmission—Mechanisms underlying the cell‐to‐cell spread of human immunodeficiency virus

Calado, M. S., Pires, D., Conceição, C. M., Santos‐Costa, Q., Anes, E., & Azevedo‐Pereira, J. M. (2023) · Reviews in Medical Virology · doi:10.1002/rmv.2480 · Cited by 8

Modulation of HIV Pathogenesis and T-cell Signaling by HIV-1 Nef

Saxena, S. K., Shrivastava, G., Tiwari, S., Swamy, M. A., & Nair, M. (2012) · Future Virology · doi:10.2217/fvl.12.42 · Cited by 8

Persistent Immune Activation in HIV-1–Infected Ex Vivo Model Tissues Subjected to Antiretroviral Therapy: Soluble and Extracellular Vesicle-Associated Cytokines

Mercurio, V., Fitzgerald, W., Molodtsov, I. A., & Margolis, L. B. (2020) · JAIDS Journal of Acquired Immune Deficiency Syndromes · doi:10.1097/qai.0000000000002301 · Cited by 8

HIV-1 Nef Impairs Heterotrimeric G-protein Signaling by Targeting Gαi2 for Degradation through Ubiquitination

Chandrasekaran, P., Buckley, M. W., Moore, V., Wang, L. Q., Kehrl, J. H., & Venkatesan, S. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.361782 · Cited by 8

Gastrointestinal germinal center B cell depletion and reduction in IgA + plasma cells in HIV-1 infection

Cossarini, F., Shang, J., Krek, A., Al-Taie, Z., Hou, R., Canales-Herrerías, P., Tokuyama, M. A., Tankelevich, M., Tillowitz, A., Jha, D., et al. (2024) · Science Immunology · doi:10.1126/sciimmunol.ado0090 · Cited by 7

HIV-1 Nef activates proviral DNA transcription by recruiting Src kinase to phosphorylate host protein Nef-associated factor 1 to compromise its viral restrictive function

Fan, T.-J., Xie, C., Li, L., Jin, X., Cui, J., & Wang, J. (2025) · Journal of Virology · doi:10.1128/jvi.00280-25 · Cited by 7

Artificial nanotube connections and transport of molecular cargo between mammalian cells

Zhang, H., Xu, S., Jeffries, G. D. M., Orwar, O., & Jesorka, A. (2013) · Nano Communication Networks · doi:10.1016/j.nancom.2013.08.006 · Cited by 7

B Lymphocyte-Derived Humoral Immune Defenses in Breast Milk Transmission of the HIV-1

Bélec, L., & Kourtis, A. P. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-2251-8_10 · Cited by 7

HIV-1–Mediated BAFF Secretion in Macrophages Does Not Require Endosomal TLRs, Type-I IFN, and Nef, but Depends on the Cellular Phenotype Status

Gomez, A. M., Ouellet, M., Deshière, A., Breton, Y., & Tremblay, M. J. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1501249 · Cited by 7

Extracellular Vesicles as a New Promising Therapy in HIV Infection

Navarrete-Muñoz, M. A., Lloréns, C., Benito, J. M., & Rallón, N. I. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.811471 · Cited by 7

Exogenous Nef Induces Proinflammatory Signaling Events in Murine Macrophages

Mangino, G., Serra, V., Borghi, P., Percario, Z. A., Horenkamp, F. A., Geyer, M., & Affabris, E. (2012) · Viral Immunology · doi:10.1089/vim.2011.0082 · Cited by 6

Tunneling Nanotubes: Intercellular Conduits for Direct Cell-to-Cell Communication in Cancer

Lou, E., & Subramanian, S. (2015) · Springer eBooks · doi:10.1007/978-94-017-7380-5_8 · Cited by 7

Employing Broadly Neutralizing Antibodies as a Human Immunodeficiency Virus Prophylactic & Therapeutic Application

Ding, C., Patel, D., Ma, Y., Mann, J. F. S., Wu, J., & Gao, Y. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.697683 · Cited by 6

Both Systemic and Mucosal LCMV Immunization Generate Robust Viral-Specific IgG in Mucosal Secretions, But Elicit Poor LCMV-Specific IgA

Rajini, B., Zeng, J., Suvas, P. K., Dech, H. M., & Onami, T. M. (2010) · Viral Immunology · doi:10.1089/vim.2010.0012 · Cited by 6

The Impact of HIV on B Cell Compartment and Its Implications for COVID-19 Vaccinations in People with HIV

Wang, L., Vulesevic, B., Vigano, M., As’sadiq, A., Kang, K., Fernández, C., Samarani, S., Anis, A. H., Ahmad, A., & Costiniuk, C. T. (2024) · Vaccines · doi:10.3390/vaccines12121372 · Cited by 7

Negative impact of HIV infection on broad-spectrum anti-HCV neutralizing antibody titers in HCV-infected patients with advanced HCV-related cirrhosis

Sepúlveda‐Crespo, D., Yélamos, B., Díez, C., Gómez, J., Hontañón, V., Torresano-Felipe, F., Berenguer, J., González‐García, J., Ibáñez, L., Llop, E., et al. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113024 · Cited by 5

HIV-1 Reverse Transcriptase Expression in HPV16-Infected Epidermoid Carcinoma Cells Alters E6 Expression and Cellular Metabolism, and Induces a Hybrid Epithelial/Mesenchymal Cell Phenotype

Сергеевна, Ж. А., Олеговна, Б. Е., Avdoshina, D., Zakirova, N. F., Frolova, G. A., Jansons, J., Chowdhury, S., Ivanov, A. V., Gordeychuk, I. V., Palefsky, J. M., et al. (2024) · Viruses · doi:10.3390/v16020193 · Cited by 5

The Mucosal B-Cell System

Brandtzæg, P., & Johansen, F. (2008) · Springer eBooks · doi:10.1007/978-1-4020-8412-6_3 · Cited by 5

Fit to deliver small RNA

Zomer, A., Vendrig, T., Hopmans, E. S., van Eijndhoven, M. A. J., Middeldorp, J. M., & Pegtel, D. M. (2010) · Cited by 5

Induction of tunnelling nanotube-like structures by influenza A viruses requires the onset of apoptosis

Weir, D., Bentley-Abbot, C., McCowan, J., Loney, C., Roberts, E. W., & Hutchinson, E. C. (2025) · PLoS Pathogens · doi:10.1371/journal.ppat.1013191 · Cited by 5

Intercellular highways of viral spread: tunneling nanotubes and extracellular vesicles at the maternal–fetal interface

Tran, L. B., Michita, R. T., Kumar, D., & Mysorekar, I. U. (2025) · Current Opinion in Virology · doi:10.1016/j.coviro.2025.101490 · Cited by 4

Extracellular vesicles: the double-edged sword in viral infections

Kumari, S., & Banerjee, A. K. (2025) · mBio · doi:10.1128/mbio.03316-25 · Cited by 4

The impact of HIV-1 Nef on CD4 + T cells

Yaseen, M. M., Abuharfeil, N. M., & Darmani, H. (2026) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2025.2599773 · Cited by 3

HIV-1 Nef Protein Affects Cytokine and Extracellular Vesicles Production in the GEN2.2 Plasmacytoid Dendritic Cell Line

Aiello, A., Giannessi, F., Percario, Z. A., Fecchi, K., Arenaccio, C., Leone, S., Carollo, M., D’Aversa, E., Chaperot, L., Gambari, R., et al. (2021) · Viruses · doi:10.3390/v14010074 · Cited by 4

Microbicides for Topical HIV Immunoprophylaxis: Current Status and Future Prospects

Zhernov, Y. V., Petrova, V. O., Simanduyev, M. Y., Shcherbakov, D. V., Полибин, Р. В., Mitrokhin, O. V., Basov, A. A., Zabroda, N. N., Высочанская, С. О., Al-khaleefa, E., et al. (2024) · Pharmaceuticals · doi:10.3390/ph17060668 · Cited by 4

Sustained Long-Term Decline in Anti-HCV Neutralizing Antibodies in HIV/HCV-Coinfected Patients Five Years after HCV Therapy: A Retrospective Study

Sepúlveda‐Crespo, D., Volpi, C., Amigot‐Sánchez, R., Yélamos, B., Díez, C., Gómez‐Gutiérrez, J., Hontañón, V., Berenguer, J., González‐García, J., Martín‐Escolano, R., et al. (2024) · Pharmaceuticals · doi:10.3390/ph17091152 · Cited by 4

HIV: implication in Burkitt lymphoma.

Tsfasman, T., Klibi, M., Pichugin, A., Lipinski, M., & Vassetzky, Y. S. (2012) · Biopolymers and Cell · doi:10.7124/bc.00005b · Cited by 4

Rapid decrease in titer and breadth of neutralizing anti-HCV antibodies in HIV/HCV-coinfected patients who achieved SVR

Vigón, L., Vázquez‐Morón, S., Berenguer, J., González‐García, J., Jiménez‐Sousa, M. Á., Guardiola, J. M., Casal, M. C., Santos, I. D. L., von Wichmann, M. Á., Carrero, A., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-48592-5 · Cited by 4

Pathobiology of CNS Human Immunodeficiency Virus Infection

Lyons, J. L., Tovar‐y‐Romo, L. B., Thakur, K. T., McArthur, J. C., & Haughey, N. J. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-398270-4.00028-8 · Cited by 3

The interplay between viruses & host microRNAs in cancer – An emerging role for HIV in oncogenesis

Mapekula, L., Ramorola, B. R., Hoosen, T. G., & Mowla, S. (2019) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2019.02.007 · Cited by 3

Regulation and Function of Mucosal IgA and IgD

Chorny, A., & Cerutti, A. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-415847-4.00032-x · Cited by 3

A imunodeficiência e o sistema imunitário: O comportamento em portadores de HIV

Soares, R., Armindo, R. D., & Rocha, G. (2014) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · Cited by 3

Mechanisms of AIDS-related Lymphoma Pathogenesis

Huysentruyt, L. C., & McGrath, M. S. (2012) · Future Virology · doi:10.2217/fvl.12.5 · Cited by 3

Host factors determine differential disease progression after infection with nef-deleted simian immunodeficiency virus

Sopper, S., Mätz‐Rensing, K., Mühl, T., Heeney, J. L., Stahl‐Hennig, C., & Sauermann, U. (2014) · Journal of General Virology · doi:10.1099/vir.0.066563-0 · Cited by 2

HIV-1 Nef Transfer and Intracellular Signalling in Uninfected Cells

Zulema, A. P., Mangino, G., Gallo, V., Chiantore, M. V., Fiorucci, G., Romeo, G., & Affabris, E. (2011) · InTech eBooks · doi:10.5772/21623 · Cited by 2

Tunneling Nanotubes in Myeloid Cells: Perspectives for Health and Infectious Diseases

Rey-Barroso, J., Dufrançais, O., & Vérollet, C. (2024) · Results and problems in cell differentiation · doi:10.1007/978-3-031-62036-2_17 · Cited by 1

Extracellular Vesicles in Viral Infections: Mechanisms, Diagnostics, and Therapeutic Perspectives for Pandemic Preparedness (SDG 3)

Govindarajan, R. K., Zaki, R. M., Kamal, M. A., Rabbee, M. F., Dhaswini, R. M., Waheeb, M. Q., Thiruvengadam, M., Kondapavuluri, B. K., & Lackner, M. K. (2025) · The EuroBiotech Journal · doi:10.2478/ebtj-2025-0015 · Cited by 1

Modeling of longitudinal immune profiles reveals distinct immunogenic signatures following five COVID-19 vaccinations among people living with HIV

Korosec, C. S., Conway, J. M., Matveev, V., Ostrowski, M., Heffernan, J. M., & Ghaemi, M. S. (2026) · Patterns · doi:10.1016/j.patter.2025.101474 · Cited by 1

SIV infection results in detrimental phenotypic and functional alterations of the naïve and memory B cell compartments that are initiated during acute infection

Kuhrt, D. M. (2010) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 1

The Mucosal Immune System

Fagarasan, S., Magri, G., & Cerutti, A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397933-9.00016-3 · Cited by 1

HIV-1/SIV Humoral Responses in External Secretions

Mestecky, J. F., & Tomaras, G. D. (2018) · Current Immunology Reviews · doi:10.2174/1573395514666180528081557 · Cited by 1

Intercellular Transport of Viral Proteins

Simon, F., & Thoma‐Kress, A. K. (2024) · Results and problems in cell differentiation · doi:10.1007/978-3-031-62036-2_18 · Cited by 1

Mucosal immunity in acute HIV: a review of recent work

Shacklett, B. L. (2025) · Current Opinion in HIV and AIDS · doi:10.1097/coh.0000000000000917 · Cited by 2

GALT CD4+PD-1hi T follicular helper (Tfh) cells repopulate after anti-retroviral therapy

Onabajo, O. O., Lewis, M. G., & Mattapallil, J. J. (2021) · Cellular Immunology · doi:10.1016/j.cellimm.2021.104396 · Cited by 1

The role of microbial translocation and gut microbiota in HIV-1 infection

Vesterbacka, J. (2017) · Figshare · Cited by 1

Mucosal Immunity in Sexually Transmitted Infections

Mestecky, J. F., & Russell, M. W. (2018) · doi:10.1002/9781119380924.ch1 · Cited by 1

AIDS virus-neutralizing antibody induction reciprocal to a PI3K gain-of-function diseasePreprint

Yamamoto, H., & Matano, T. (2023) · eLife · doi:10.7554/elife.88849.1 · Cited by 1

SIV-specific neutralizing antibody induction following selection of a PI3K drive-attenuated nef variantPreprint

Yamamoto, H., & Matano, T. (2023) · eLife · doi:10.7554/elife.88849 · Cited by 1

Influenza A viruses induce tunnelling nanotube-like structures through the onset of apoptosisPreprint

Weir, D., Bentley-Abbot, C., McCowan, J., Loney, C., Roberts, E. W., & Hutchinson, E. C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.25.614890 · Cited by 1

Tunneling nanotube networks in dendritic cell communication and HIV-1 trans-infection

Zaccard, C. R. (2015) · D-Scholarship@Pitt (University of Pittsburgh)

Functions of the Lentiviral Accessory Protein Nef During the Distinct Steps of HIV and SIV Replication Cycle

Luciana, J., Luiza, M., & Thatiane, L. (2011) · InTech eBooks · doi:10.5772/23519

Seeking a mechanism of action for the anti-HIV properties of the CD8 antiviral factor, CAF

Shridhar, V. (2011) · D-Scholarship@Pitt (University of Pittsburgh)

HIV-1 Persistence in Macrophage Reservoirs during Antiretroviral Therapy

Lamers, S. L., & McGrath, M. S. (2014)

HIV-1 NEF: THERAPEUTIC STRATEGIES AND VIROLOGICAL SYNAPSE-MEDIATED INFECTION

Green, L. A. (2011) · IUScholarWorks (Indiana University) · doi:10.7912/c2/1705

Role of HIV-1 Nef and Vpu in viral replication and CD4+ T cell depletion.

Watkins, R. L. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/37jt-7j98

Analytic and integrative perspectives for HIV vaccine design

Yamamoto, H. (2013) · Uirusu · doi:10.2222/jsv.63.219

HIV-1 NEF: THERAPEUTIC STRATEGIES AND VIROLOGICAL

Green, L. A. (2010)

Dynamics of memory B-cell populations in blood, lymph node and bone marrow during

Demberg, T., Brocca‐Cofano, E., Xiao, P., Venzon, D. J., Vargas, D., Lee, E. M., Kalisz, I., Kalyanaraman, V. S., DiPasquale, J., & Robert-Guroff, M. (2012)

Viral and Host Determinants of HIV-1 Disease Progression

Schuitemaker, H., & Wout, A. B. V. ’. (2008) · Elsevier eBooks · doi:10.1016/b978-1-4160-2882-6.50009-5

Investigation of B cell subsets and vaccination responses in HIV-1 infection and CVID

Hart, M. (2011) · Spiral (Imperial College London) · doi:10.25560/9328

PHAGOCYTES, GRANULOCYTES, AND MYELOPOIESIS HIV-1 reprograms the migration of macrophages

Souriant, S., Bonnaud, E. M., Jolicoeur, P., Raynaud‐Messina, B., Kinnaer, C., Fourquaux, I., Imle, A., Bénichou, S., Fackler, O., Poincloux, R., et al. (2017)

Evaluation of Mucosal Humoral and Cellular Immune Responses to HIV in External Secretions and Mucosal Tissues

Sabbaj, S., & Mestecky, J. F. (2018) · Current Immunology Reviews · doi:10.2174/1573395514666180621152303

The role of tunneling nanotubes in mediating intercellular communication in cancer

Desir, S. (2018) · University of Minnesota Digital Conservancy (University of Minnesota)

Viral and host determinants of HIV-1 disease progression

van Manen, D., Wout, A. B. V. ’., & Schuitemaker, H. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4557-0695-2.00005-5

Study of Tunneling Nanotubes Based on Co-Culture System of Human and Mouse Cells

姚, 伟. (2020) · Bioprocess · doi:10.12677/bp.2020.104006

Faculty Opinions recommendation of Tunneling nanotubes provide a unique conduit for intercellular transfer of cellular contents in human malignant pleural mesothelioma.

Sethi, T., & Rooney, C. (2013) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.717954412.793469193

Pathobiology of CNS human immunodeficiency virus infection

Rubin, L. H., Tovar‐y‐Romo, L. B., & Haughey, N. J. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-85654-6.00031-9

Regulation of Blood-Testis Barrier (BTB) proteins in Sertoli-germ cell nanotube formation in EF-treated spermatogenesisPreprint

Güngör‐Ordueri, N. E., Elgün, T., Özgürses, M. E., Uzunkaya, B., & Tasdemir, M. (2022) · Research Square · doi:10.21203/rs.3.rs-2357692/v1

Features of the immune status in HIV-infected patients with Kaposi’s sarcoma

Khryanin, А. А., Sturov, V. G., Aivazian, G. A., Bezhetskikh, R. S., & Pushkarev, E. V. (2023) · Russian Journal of Clinical Dermatology and Venereology · doi:10.17116/klinderma202322021130

SIV-Specific Neutralizing Antibody Induction Following Selection of a T-Cell Escape nef Mutation

Yamamoto, H., & Matano, T. (2019) · eLife · doi:10.7554/elife.88849.4

Tunneling nanotubes

Edgünlü, T., & Özdemir, Ç. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-18858-9.00005-6

Intercellular Highways in Transport Processes

Szabó‐Meleg, E. (2024) · Results and problems in cell differentiation · doi:10.1007/978-3-031-62036-2_9

SIV-specific neutralizing antibody induction following selection of a PI3K drive-attenuated nef variantPreprint

Yamamoto, H., & Matano, T. (2024) · eLife · doi:10.7554/elife.88849.2

SIV-specific neutralizing antibody induction following selection of a PI3K drive-attenuated nef variantPreprint

Yamamoto, H., & Matano, T. (2025) · eLife · doi:10.7554/elife.88849.3

Machine Learning Reveals Distinct Immunogenic Signatures of Th1 Imprinting in ART-Treated Individuals with HIV Following Repeated SARS-CoV-2 VaccinationPreprint

Korosec, C. S., Conway, J. M., Matveev, V., Ostrowski, M., Heffernan, J. M., & Ghaemi, M. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.18.643769 · Cited by 1

HIV-1 Reprograms CD4 T Cell Responses by Impairing Antigen-specific Communication with Dendritic CellsPreprint

Morath, K., Stolp, B., Rosenbauer, J., Mahnke, K., Platten, M., & Fackler, O. (2025) · SSRN Electronic Journal · doi:10.1101/2025.08.14.670333

GB virus C interactions with HIV

Bhattarai, N. (2013) · doi:10.17077/etd.qcvau1en

Association entre les dérégulations des cellules dendritiques et les altérations des lymphocytes B présentes chez les patients infectés par le VIH

Fontaine, J. (2010) · doi:10.71781/28279

A Novel Motif in HIV-1 Nef that Regulates MIP-1β Chemokine Release in Macrophages: A Dissertation

Dai, L. (2010) · eScholarship@UMassChan · doi:10.13028/gwmf-s887

Additional file 1 of M-Sec facilitates intercellular transmission of HIV-1 through multiple mechanisms

Lotfi, S. E., Nasser, H., Noyori, O., Hiyoshi, M., Takeuchi, H., Koyanagi, Y., & Suzu, S. (2020) · Figshare · doi:10.6084/m9.figshare.12643775

Rôle des macrophages au cours de l'infection par le VIH-1 et dans un contexte de co-infection avec Mycobacterium tuberculosis

Souriant, S. (2017) · theses.fr (ABES) · doi:10.70675/1508e6c1zc271z49c7z80eez7d9af58ba3f5

Étude de la propagation prion-like de l'alpha-synucléine dans des réseaux de neurones reconstruits

Courte, J. (2019) · theses.fr (ABES) · doi:10.70675/95ccfbd6zedb2z4a1bz8024zb46a3ec60ebf

Architecture of Tunneling Nanotubes : a Structural Approach

Cervantes, D. C. (2019) · theses.fr (ABES) · doi:10.70675/7134eee8z8acdz4e45za0afz00069cdc5443

Tunneling Nanotubes and their role in Glioblastoma Treatment-Resistance

Pinto, G. (2020) · theses.fr (ABES) · doi:10.70675/c0be4194z66c1z449az9503ze776ac13b855

Identification of novel factors involved in the exacerbation of HIV-1 infection and spread among macrophages in the tuberculosis context

Dupont, M. (2019) · theses.fr (ABES) · doi:10.70675/a9860843z73b2z4e66zb7d6z858eb79b6cf3

IL-33/ST2 and tissue Treg/AREG pathways in the pathophysiology of HIV infection

Tariq, M. (2021) · theses.fr (ABES) · doi:10.70675/749fcf56zf271z4375zbcb4zfe8a07253724

Etude de la transmission intercellulaire du VIH-1 vers les macrophages par fusion cellule-cellule

Mascarau, R. (2022) · theses.fr (ABES) · doi:10.70675/2e3aacaazcd4fz49a5zb350zcd4933447d78

Rôle des virus EBV et VIH dans la formation de la translocation chromosomique t(8;14) du Lymphome de Burkitt

Sall, F. B. (2021) · theses.fr (ABES) · doi:10.70675/4ade78c4z0bf6z4533zb4a6z084522268290

HIV-1 entry co-receptor usage and cell-tropism during cell-to-cell transfer and dissemination in macrophage

Han, M. (2022) · theses.fr (ABES) · doi:10.70675/439e8f1azc09cz4c87z9b3fz88c721e1a5b5

110 Nef-Trafficking Intercellular Highways for HIV Evasion of Antibody Production

Xu, W., Santini, P. A., Sullivan, J. S., He, B., Shan, M., Ball, S. C., Dyer, W. B., Ketas, T. J., Chadburn, A., Cohen‐Gould, L., et al. (2011) · JAIDS Journal of Acquired Immune Deficiency Syndromes · doi:10.1097/01.qai.0000397300.56223.a7

Long‐Distance Tunneling Nanotubules Shuttle Immunoglobulin Class Switch‐Suppressing Factors from HIV‐Infected Macrophages to B Cells

Xu, W., Santini, P. A., Shan, M., Chen, K., Ball, S. C., Chiu, A., Kingsley, L., Rinaldo, C. R., Chadburn, A., Knowles, D. M., et al. (2008) · The FASEB Journal · doi:10.1096/fasebj.22.1_supplement.856.26

Long-Distance Commuting

Mueller, K. L. (2009) · Science · doi:10.1126/science.325_1477a · Cited by 3

Intrusive HIV-1-infected cells

Rudnicka, D., & Schwartz, O. (2009) · Nature Immunology · doi:10.1038/ni0909-933 · Cited by 33

Long-Distance Tunneling Nanotubules Shuttle Viral Immunoglobulin Class Switch-Suppressing Factors from HIV-Infected Macrophages to B Cells.

Xu, W., Santini, P. A., Shan, M., Chen, K., Ball, S. C., Chiu, A., Kingsley, L., Rinaldo, C. R., Chadburn, A., Knowles, D. M., et al. (2007) · Blood · doi:10.1182/blood.v110.11.2278.2278