What Is the most Important for Elite Control: Genetic Background of Patient, Genetic Background of Partner, both or neither? Description of Complete Natural History within a Couple of MSM
M. Bendenoun,
A. Samri,
V. Avettand-Fènoël,
S. Cardinaud,
B. Descours,
G. Carcelain,
M.-C. Mazeron,
J.-F. Bergmann,
A. Urrutia,
A. Moris,
C. Rouzioux,
F. Simon,
P. Andre,
M. Pocard,
X. Dray,
T. Mourez,
V. Vieillard,
B. Autran,
F. Barin,
P. Sellier
Affiliations
M. Bendenoun
Département de Médecine Interne, Groupe Hospitalier Saint-Louis-Lariboisière-Fernand Widal, APHP, Paris, France
A. Samri
U1135, CIMI, INSERM, Paris, France
V. Avettand-Fènoël
EA7327, Faculté de Médecine, Université Paris-Descartes, Sorbonne Paris Cité, France
S. Cardinaud
U1135, CIMI, INSERM, Paris, France
B. Descours
U1135, CIMI, INSERM, Paris, France
G. Carcelain
U1135, CIMI, INSERM, Paris, France
M.-C. Mazeron
Laboratoire de Virologie, Groupe Hospitalier Saint-Louis-Lariboisière-Fernand Widal, APHP, Paris, France.
J.-F. Bergmann
Département de Médecine Interne, Groupe Hospitalier Saint-Louis-Lariboisière-Fernand Widal, APHP, Paris, France
A. Urrutia
U1135, CIMI, INSERM, Paris, France
A. Moris
U1135, CIMI, INSERM, Paris, France
C. Rouzioux
EA7327, Faculté de Médecine, Université Paris-Descartes, Sorbonne Paris Cité, France
F. Simon
Laboratoire de Virologie, Groupe Hospitalier Saint-Louis-Lariboisière-Fernand Widal, APHP, Paris, France.
P. Andre
CIRI, INSERM U1111, CNRS UMR5308, Université Lyon 1, ENS de Lyon, Lyon, France
M. Pocard
Service de Chirurgie Digestive et Cancérologique, Groupe Hospitalier Saint-Louis-Lariboisière-Fernand Widal, APHP, Paris, France
X. Dray
Service de Gastroentérologie, Groupe Hospitalier Saint-Louis-Lariboisière-Fernand Widal, APHP, Paris, France.
T. Mourez
Normandie Univ, UNIROUEN, EA 2656, Rouen University Hospital, Department of Virology, F-76000 Rouen, France
V. Vieillard
U1135, CIMI, INSERM, Paris, France
B. Autran
U1135, CIMI, INSERM, Paris, France
F. Barin
Inserm U966 & National Reference Center for HIV, Université François-Rabelais & CHU Bretonneau, Tours, France
P. Sellier
Département de Médecine Interne, Groupe Hospitalier Saint-Louis-Lariboisière-Fernand Widal, APHP, Paris, France
Background: We describe a homosexual man who strongly controlled HIV-1 for ten years despite lack of protective genetic background. Methods: HIV-1 DNA was measured in blood and other tissues. Cell susceptibility was evaluated with various strains. HIV-1-specific (CD4 and CD8 activation markers and immune check points) and NK cells responses were assessed; KIRs haplotypes and HLA alleles were determined. Findings: Two HIV-1 RNA copies/mL of plasma were detected in 2009, using an ultra-sensitive assay. HIV-DNA was detected at 1.1 and 2 copies/106 PBMCs in 2009 and 2015 respectively, at 1.2 copies/106 cells in rectal cells in 2011. WBs showed weak reactivity with antibodies to gp160, p55 and p25 from 2007 to 2014, remaining incomplete in 2017. CD4 T cells were susceptible to various strains including HIVKON, a primary isolate of his own CRF02_AG variant. CD8 T cells showed a strong poly-functional response against HIV-Gag, producing mainly IFN-γ; a robust capacity of antibody-dependant cell cytotoxicity (ADCC) was observed in NK cells. Case patient was group B KIR haplotype. Neutralizing antibodies were not detected. CD4 and CD8 blood T cells showed normal proportions without increased activation markers. Phylogenetic analyses identified the same CRF02_AG variant in his partner. The patient and his partner were heterozygous for the CCR5ΔD32 deletion and shared HLA-B*07, C*07 non-protective alleles. Interpretation: This thorough description of the natural history of an individual controlling HIV-1 in various compartments for ten years despite lack of protective alleles, and of his partner, may have implications for strategies to cure HIV-1 infection.