10.3389/fimmu.2019.00408.s005
Celestine N. Wanjalla
Celestine
N. Wanjalla
Wyatt J. McDonnell
Wyatt J.
McDonnell
Louise Barnett
Louise
Barnett
Joshua D. Simmons
Joshua D.
Simmons
Briana D. Furch
Briana D.
Furch
Morgan C. Lima
Morgan C.
Lima
Beverly O. Woodward
Beverly O.
Woodward
Run Fan
Run
Fan
Ye Fei
Ye
Fei
Paxton G. Baker
Paxton G.
Baker
Ramesh Ram
Ramesh
Ram
Mark A. Pilkinton
Mark A.
Pilkinton
Mona Mashayekhi
Mona
Mashayekhi
Nancy J. Brown
Nancy J.
Brown
Simon A. Mallal
Simon A.
Mallal
Spyros A. Kalams
Spyros
A. Kalams
John R. Koethe
John
R. Koethe
Image_2_Adipose Tissue in Persons With HIV Is Enriched for CD4+ T Effector Memory and T Effector Memory RA+ Cells, Which Show Higher CD69 Expression and CD57, CX3CR1, GPR56 Co-expression With Increasing Glucose Intolerance.TIFF
Frontiers
2019
HIV—human immunodeficiency virus
adipose tissue
diabetes mellitus
TEMRA
T effector memory cells
GPR56
CX3CR1
memory T cells
2019-03-19 04:44:30
Figure
https://frontiersin.figshare.com/articles/figure/Image_2_Adipose_Tissue_in_Persons_With_HIV_Is_Enriched_for_CD4_T_Effector_Memory_and_T_Effector_Memory_RA_Cells_Which_Show_Higher_CD69_Expression_and_CD57_CX3CR1_GPR56_Co-expression_With_Increasing_Glucose_Intolerance_TIFF/7860560
<p>Chronic T cell activation and accelerated immune senescence are hallmarks of HIV infection, which may contribute to the increased risk of cardiometabolic diseases in people living with HIV (PLWH). T lymphocytes play a central role in modulating adipose tissue inflammation and, by extension, adipocyte energy storage and release. Here, we assessed the CD4<sup>+</sup> and CD8<sup>+</sup> T cell profiles in the subcutaneous adipose tissue (SAT) and blood of non-diabetic (n = 9; fasting blood glucose [FBG] < 100 mg/dL), pre-diabetic (n = 8; FBG = 100–125 mg/dL) and diabetic (n = 9; FBG ≥ 126 mg/dL) PLWH, in addition to non- and pre-diabetic, HIV-negative controls (n = 8). SAT was collected by liposuction and T cells were extracted by collagenase digestion. The proportion of naïve (T<sub>Nai</sub>) CD45RO<sup>−</sup>CCR7<sup>+</sup>, effector memory (T<sub>EM</sub>) CD45RO<sup>+</sup>CCR7<sup>−</sup>, central memory (T<sub>CM</sub>) CD45RO<sup>+</sup>CCR7<sup>+</sup>, and effector memory revertant RA<sup>+</sup>(T<sub>EMRA</sub>) CD45RO<sup>−</sup>CCR7<sup>−</sup> CD4<sup>+</sup> and CD8<sup>+</sup> T cells were measured by flow cytometry. CD4<sup>+</sup> and CD8<sup>+</sup> T<sub>EM</sub> and T<sub>EMRA</sub> were significantly enriched in SAT of PLWH compared to blood. The proportions of SAT CD4<sup>+</sup> and CD8<sup>+</sup> memory subsets were similar across metabolic status categories in the PLWH, but CD4<sup>+</sup> T cell expression of the CD69 early-activation and tissue residence marker, particularly on T<sub>EM</sub> cells, increased with progressive glucose intolerance. Use of t-distributed Stochastic Neighbor Embedding (t-SNE) identified a separate group of predominantly CD69<sup>lo</sup> T<sub>EM</sub> and T<sub>EMRA</sub> cells co-expressing CD57, CX<sub>3</sub>CR1, and GPR56, which were significantly greater in diabetics compared to non-diabetics. Expression of the CX<sub>3</sub>CR1 and GPR56 markers indicate these T<sub>EM</sub> and T<sub>EMRA</sub> cells may have anti-viral specificity. Compared to HIV-negative controls, SAT from PLWH had an increased CD8:CD4 ratio, but the distribution of CD4<sup>+</sup> and CD8<sup>+</sup> memory subsets was similar irrespective of HIV status. Finally, whole adipose tissue from PLWH had significantly higher expression of TLR2, TLR8, and multiple chemokines potentially relevant to immune cell homing compared to HIV-negative controls with similar glucose tolerance.</p>