National Cancer Institute (NCI), Bethesda; San Raffaele Scientific Institute, Milan; University of Cagliari; National Institute of Allergy and Infectious Diseases (NIAID), Bethesda
Paolo Lusso is an Italian doctor and scientist who specializes in virology and immunology. He is the Chief of the Viral Pathogenesis Section at the Laboratory of Immunoregulation and Infectious Diseases of the National Institute of Allergy and Infectious Diseases (NIAID) in Bethesda, Maryland, US. He is best known for his 1995 discovery of three chemokines (chemotactic cytokines) that naturally block HIV-1, RANTES, MIP-1α and MIP-1β, which inaugurated the field of HIV and chemokines.
Lusso's major scientific accomplishments include the establishment of the first connection between the fields of HIV-1 and the chemokine system with the discovery of three chemokines that naturally block HIV-1 (i.e., RANTES, MIP-1α and MIP-1β; cited nearly 4,000 times according to Google Scholar), the elucidation of multiple mechanisms of interaction between the CD4+ T-lymphotropic human herpesvirus HHV-6 and HIV-1, the in-vitro and in-vivo characterization of chemokine receptor usage by HIV-1, the identification of the cellular receptors for HHV-6 and HHV-7, the discovery of a second receptor (CD4)-binding site for HIV-1, and the development of a protective mRNA vaccine against HIV-1 (in collaboration with Moderna; featured on the cover page of the journal Nature Medicine). The HIV-1 vaccine designed by Lusso utilizes mRNA to instruct the body to produce virus-like particles (VLPs), which closely mimic real-life HIV-1 virions (albeit lacking infectivity) and, thereby, induce more effective immune responses. It has demonstrated protective efficacy in rhesus macaques.
Awards and recognitions
"Breakthrough of the Year" (for the discovery of HIV-suppressive chemokines), Science, Washington, D.C. (USA), 1996.
↑D'Souza, M. Patricia; Harden, Victoria (December 1996). "Chemokines and HIV–1 second receptors". Nature Medicine. 2 (12): 1293–1300. doi:10.1038/nm1296-1293. PMID8946819.
↑Balter, Michael (8 December 1995). "Elusive HIV-Suppressor Factors Found: Three factors, secreted by immune system cells, that apparently work in concert to suppress HIV replication have been identified after a long search; a fourth molecule may also be involved". Science. 270 (5242): 1560–1561. doi:10.1126/science.270.5242.1560. PMID7502059.
↑Cocchi, Fiorenza; DeVico, Anthony L.; Garzino-Demo, Alfredo; Arya, Suresh K.; Gallo, Robert C.; Lusso, Paolo (15 December 1995). "Identification of RANTES, MIP-1α, and MIP-1β as the Major HIV-Suppressive Factors Produced by CD8 + T Cells". Science. 270 (5243): 1811–1815. Bibcode:1995Sci...270.1811C. doi:10.1126/science.270.5243.1811. PMID8525373.
↑Lusso, P; Ensoli, B; Markham, PD; Ablashi, DV; Salahuddin, SZ; Tschachler, E; Wong-Staal, F; Gallo, RC (26 January 1989). "Productive dual infection of human CD4+ T lymphocytes by HIV-1 and HHV-6". Nature. 337 (6205): 370–3. doi:10.1038/337370a0. PMID2463490.
↑Lusso, P; De Maria, A; Malnati, M; Lori, F; DeRocco, SE; Baseler, M; Gallo, RC (7 February 1991). "Induction of CD4 and susceptibility to HIV-1 infection in human CD8+ T lymphocytes by human herpesvirus 6". Nature. 349 (6309): 533–5. doi:10.1038/349533a0. PMID1846951.
↑Lusso, P; Malnati, MS; Garzino-Demo, A; Crowley, RW; Long, EO; Gallo, RC (1 April 1993). "Infection of natural killer cells by human herpesvirus 6". Nature. 362 (6419): 458–62. Bibcode:1993Natur.362..458L. doi:10.1038/362458a0. PMID7681936.
↑Scarlatti, G; Tresoldi, E; Björndal, A; Fredriksson, R; Colognesi, C; Deng, HK; Malnati, MS; Plebani, A; Siccardi, AG; Littman, DR; Fenyö, EM; Lusso, P (November 1997). "In vivo evolution of HIV-1 co-receptor usage and sensitivity to chemokine-mediated suppression". Nature Medicine. 3 (11): 1259–65. doi:10.1038/nm1197-1259. PMID9359702.
↑Cocchi, F; DeVico, AL; Garzino-Demo, A; Cara, A; Gallo, RC; Lusso, P (November 1996). "The V3 domain of the HIV-1 gp120 envelope glycoprotein is critical for chemokine-mediated blockade of infection". Nature Medicine. 2 (11): 1244–7. doi:10.1038/nm1196-1244. PMID8898753.