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1.
PLoS Pathog ; 17(4): e1009536, 2021 04.
Artigo em Inglês | MEDLINE | ID: mdl-33905459

RESUMO

Skin mononuclear phagocytes (MNPs) provide the first interactions of invading viruses with the immune system. In addition to Langerhans cells (LCs), we recently described a second epidermal MNP population, Epi-cDC2s, in human anogenital epidermis that is closely related to dermal conventional dendritic cells type 2 (cDC2) and can be preferentially infected by HIV. Here we show that in epidermal explants topically infected with herpes simplex virus (HSV-1), both LCs and Epi-cDC2s interact with HSV-1 particles and infected keratinocytes. Isolated Epi-cDC2s support higher levels of infection than LCs in vitro, inhibited by acyclovir, but both MNP subtypes express similar levels of the HSV entry receptors nectin-1 and HVEM, and show similar levels of initial uptake. Using inhibitors of endosomal acidification, actin and cholesterol, we found that HSV-1 utilises different entry pathways in each cell type. HSV-1 predominantly infects LCs, and monocyte-derived MNPs, via a pH-dependent pathway. In contrast, Epi-cDC2s are mainly infected via a pH-independent pathway which may contribute to the enhanced infection of Epi-cDC2s. Both cells underwent apoptosis suggesting that Epi-cDC2s may follow the same dermal migration and uptake by dermal MNPs that we have previously shown for LCs. Thus, we hypothesize that the uptake of HSV and infection of Epi-cDC2s will stimulate immune responses via a different pathway to LCs, which in future may help guide HSV vaccine development and adjuvant targeting.


Assuntos
Herpesvirus Humano 1/fisiologia , Células de Langerhans/virologia , Internalização do Vírus , Adolescente , Animais , Células Cultivadas , Criança , Pré-Escolar , Chlorocebus aethiops , Epiderme/patologia , Epiderme/virologia , Células HaCaT , Células HeLa , Herpes Simples/patologia , Herpes Simples/virologia , Humanos , Lactente , Transdução de Sinais/fisiologia , Células Vero
2.
Plast Reconstr Surg ; 141(3): 637-645, 2018 03.
Artigo em Inglês | MEDLINE | ID: mdl-29481394

RESUMO

BACKGROUND: The authors studied the incidence of low back pain and urinary incontinence in the postpartum population presenting for abdominoplasty, and the extent of improvement following the operation. METHODS: This multicenter prospective study used validated questionnaires: the Oswestry Disability Index for back pain and the International Consultation on Incontinence Questionnaire-Urinary Incontinence-Short Form for urinary incontinence. Questionnaires were administered preoperatively and at 6 weeks and 6 months postoperatively. RESULTS: Results cover 214 patients from nine centers. The mean age was 42.1 years, the mean parity was 2.5, and the mean body mass index was 26.3 kg/m. The mean surgical statistics were as follows: weight removed, 1222 g; liposuction volume, 795 ml; and diastasis, 4.5 cm. Eighty-seven percent of the abdominoplasties were either radical, high lateral tension, or high oblique tension. The mean Oswestry Disability Index score preoperatively was 21.6 percent, and 8.8 percent had no back pain. The mean score was 8 percent at 6 weeks and 3.2 percent at 6 months. These results are statistically significant. The mean International Consultation on Incontinence Questionnaire score preoperatively was 6.5; of the patients assessed, 27.5 percent had no incontinence. This score fell to 1.6 at 6 weeks, and the same, 1.6, at 6 months. These results are also statistically significant. Preoperative predictors of back pain were body mass index greater than 25 kg/m and umbilical hernia; predictors of incontinence were age older than 40 years and vaginal deliveries. There were no significant predictors of postoperative back pain or urinary incontinence improvement at 6 months. All methods of abdominoplasty produced similar improvement. CONCLUSION: Abdominoplasty with rectus repair creates a significant improvement in the functional symptoms of low back pain and urinary incontinence. CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, IV.


Assuntos
Abdominoplastia/métodos , Dor Lombar/cirurgia , Incontinência Urinária/cirurgia , Adulto , Avaliação da Deficiência , Feminino , Humanos , Dor Lombar/prevenção & controle , Paridade , Gravidez , Complicações na Gravidez/cirurgia , Inquéritos e Questionários , Resultado do Tratamento
3.
Plast Reconstr Surg ; 135(2): 319-329, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25383716

RESUMO

BACKGROUND: Biofilm infection of breast implants significantly potentiates capsular contracture. This study investigated whether chronic biofilm infection could promote T-cell hyperplasia. METHODS: In the pig study, 12 textured and 12 smooth implants were inserted into three adult pigs. Implants were left in situ for a mean period of 8.75 months. In the human study, 57 capsules from patients with Baker grade IV contracture were collected prospectively over a 4-year period. Biofilm and surrounding lymphocytes were analyzed using culture, nucleic acid, and visualization techniques. RESULTS: In the pig study, all samples were positive for bacterial biofilm. There was a significant correlation between the bacterial numbers and grade of capsular contracture (p = 0.04). Quantitative real-time polymerase chain reaction showed that all lymphocytes were significantly more numerous on textured compared with smooth implants (p < 0.001). T cells accounted for the majority of the lymphocytic infiltrate. Imaging confirmed the presence of activated lymphocytes. In the human study, all capsules were positive for biofilm. Analysis of lymphocyte numbers showed a T-cell predominance (p < 0.001). There was a significant linear correlation between the number of T and B cells and the number of detected bacteria (p < 0.001). Subset analysis showed a significantly higher number of bacteria for polyurethane implants (p < 0.005). CONCLUSIONS: Chronic biofilm infection around breast prostheses produces an increased T-cell response both in the pig and in humans. A possible link between bacterial biofilm and T-cell hyperplasia is significant in light of breast implant-associated anaplastic large-cell lymphoma. CLINICAL QUESTION/LEVEL OF EVIDENCE: Risk, V.


Assuntos
Biofilmes , Implantes de Mama/efeitos adversos , Contratura Capsular em Implantes/imunologia , Linfoma Anaplásico de Células Grandes/etiologia , Infecções Relacionadas à Prótese/imunologia , Subpopulações de Linfócitos T/imunologia , Adulto , Animais , Linfócitos B/imunologia , Biofilmes/crescimento & desenvolvimento , Doença Crônica , Feminino , Humanos , Hiperplasia , Contratura Capsular em Implantes/epidemiologia , Contratura Capsular em Implantes/microbiologia , Contratura Capsular em Implantes/cirurgia , Ativação Linfocitária , Microscopia Confocal , Poliuretanos , Infecções Relacionadas à Prótese/patologia , Reação em Cadeia da Polimerase em Tempo Real , Método Simples-Cego , Sus scrofa , Suínos
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