Publications by authors named "Meei Li Huang"

Article Synopsis
  • The study investigates the immune response to HSV-2 reactivation by examining T cells in skin biopsies and blood samples before and after vaccination with an HSV-2 candidate vaccine (HSV529).
  • After the first vaccine dose, there was a notable increase in HSV-2-specific CD4+ T cell sequences from blood that made their way into the skin, indicating a successful immune memory response.
  • Unique T cell clones were identified in the skin that weren't found in the blood, suggesting that the skin has a distinct immune profile, and highlights the importance of studying tissue-specific immunity in vaccine responses.
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Article Synopsis
  • Anti-HSV therapies currently only suppress the virus and don't eliminate its dormant form in nerve cells, which causes recurring outbreaks.
  • A new gene editing method using HSV-specific meganucleases delivered by adeno-associated virus (AAV) can significantly reduce latent HSV DNA in mouse models, achieving over 90% elimination in orofacial infections and up to 97% in genital infections.
  • Although the therapy is mostly well-tolerated, some high doses lead to liver toxicity and mild nerve damage; adjustments like using a single AAV serotype and a specific neuron-targeting promoter could enhance safety without losing effectiveness.
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Background: Although antivirals remain important for the treatment COVID-19, methods to assess treatment efficacy are lacking. Here, we investigated the impact of remdesivir on viral dynamics and their contribution to understanding antiviral efficacy in the multicenter Adaptive COVID-19 Treatment Trial 1, which randomized patients to remdesivir or placebo.

Methods: Longitudinal specimens collected during hospitalization from a substudy of 642 patients with COVID-19 were measured for viral RNA (upper respiratory tract and plasma), viral nucleocapsid antigen (serum), and host immunologic markers.

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The skin at the site of HSV-2 reactivation is enriched for HSV-2-specific T cells. To evaluate whether an immunotherapeutic vaccine could elicit skin-based memory T cells, we studied skin biopsies and HSV-2-reactive CD4 T cells from peripheral blood mononuclear cells (PBMCs) by T cell receptor β () sequencing before and after vaccination with a replication-incompetent whole virus HSV-2 vaccine candidate (HSV529). The representation of HSV-2-reactive CD4 sequences from PBMCs in the skin repertoire increased after the first vaccine dose.

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Limited understanding of the immunopathogenesis of human herpesvirus 6B (HHV-6B) has prevented its acceptance as a pulmonary pathogen after hematopoietic cell transplant (HCT). In this prospective multicenter study of patients undergoing bronchoalveolar lavage (BAL) for pneumonia after allogeneic HCT, we test blood and BAL fluid (BALF) for HHV-6B DNA and mRNA transcripts associated with lytic infection and perform RNA-seq on paired blood. Among 116 participants, HHV-6B DNA is detected in 37% of BALs, 49% of which also have HHV-6B mRNA detection.

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Article Synopsis
  • The study investigates the relationship between host gene expression and the HIV reservoir in people with HIV who are on antiretroviral therapy, identifying key genes associated with both smaller and larger viral reservoirs.
  • Higher expression of tumor suppressor genes P3H3 and NBL1 correlates with a smaller total DNA viral reservoir, while lower expression of 17 other host genes, including those related to membrane channels and innate immunity, is linked to higher levels of HIV transcription.
  • The research also highlights significant gene signaling pathways involved in HIV persistence and introduces potential biomarkers for targeting the HIV reservoir, making it one of the largest studies of its kind.
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Background: Antiviral resistance in human herpes simplex viruses (HSV) remains a significant clinical challenge in immunocompromised populations. Although molecular tests have largely replaced viral culture for HSV diagnosis and molecular antiviral resistance testing is available for many viruses, HSV resistance testing continues to rely on phenotypic, viral culture-based methods, requiring weeks for results. Consequently, treatment of suspected HSV resistance remains largely empiric.

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Background: Co-infection with HIV can result in impaired control of cytomegalovirus (CMV) replication, increasing the likelihood of disease and onward transmission. The objective of this analysis was to measure the impact of HIV on CMV replication in an intensively-sampled cohort in Kampala, Uganda.

Methods: CMV seropositive men and women aged 18-65, with or without HIV co-infection, were followed for one month.

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  • The study explores the effects of letermovir on the use of anti-CMV therapy and HHV-6 incidence in allogeneic HCT patients, indicating a significant reduction in broad-spectrum antiviral use post-letermovir.
  • Analysis of 738 patients showed no significant change in the cumulative incidence of HHV-6 testing and detection between pre- and post-letermovir groups, with only minor differences in HHV-6-related conditions.
  • Overall, despite the reduced use of broad-spectrum antivirals due to letermovir implementation, HHV-6 epidemiology remained stable, with no significant associations found related to HHV-6 detection rates.
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Background: Remdesivir is approved for treatment of coronavirus disease 2019 (COVID-19) in nonhospitalized and hospitalized adult and pediatric patients. Here we present severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) resistance analyses from the phase 3 ACTT-1 randomized placebo-controlled trial conducted in adult participants hospitalized with COVID-19.

Methods: Swab samples were collected at baseline and longitudinally through day 29.

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HIV-specific T cells are necessary for control of HIV-1 replication but are largely insufficient for viral clearance. This is due in part to these cells' recognition of immunodominant but variable regions of the virus, which facilitates viral escape mutations that do not incur viral fitness costs. HIV-specific T cells targeting conserved viral elements are associated with viral control but are relatively infrequent in people living with HIV (PLWH).

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Hepatitis B virus (HBV) is a pathogen of major public health importance that is largely incurable once a chronic infection is established. Only humans and great apes are fully permissive to HBV infection, and this species restriction has impacted HBV research by limiting the utility of small animal models. To combat HBV species restrictions and enable more studies, liver-humanized mouse models have been developed that are permissive to HBV infection and replication.

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Background And Aims: Adeno-associated virus (AAV) vectors are widely used to deliver therapeutic transgenes to distinct tissues, including the liver. Vectors based on naturally occurring AAV serotypes as well as vectors using engineered capsids have shown variations in tissue tropism and level of transduction between different mouse models. Moreover, results obtained in rodents frequently lack translatability into large animal studies.

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Mucosal infections pose a significant global health burden. Antigen-specific tissue-resident T cells are critical to maintaining barrier immunity. Previous studies in the context of systemic infection suggest that memory CD8+ T cells may also provide innate-like protection against antigenically unrelated pathogens independent of T cell receptor engagement.

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Article Synopsis
  • The study investigates genetic factors that influence the persistence of HIV-infected cells in individuals on antiretroviral therapy (ART), focusing on those who do not naturally control the virus (non-controllers).
  • It highlights that lower levels of HIV total DNA in CD4+ T cells are linked to the upregulation of tumor suppressor genes, while higher levels of HIV unspliced RNA relate to downregulation of inflammatory and immune-related genes.
  • The research indicates that inflammation, immune responses, and tumor suppression are important in understanding how the HIV reservoir is maintained in treated individuals, suggesting further studies are needed to confirm these results.
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Objective: Prior genomewide association studies have identified variation in major histocompatibility complex (MHC) class I alleles and C-C chemokine receptor type 5 gene (CCR5Δ32) as genetic predictors of viral control, especially in 'elite' controllers, individuals who remain virally suppressed in the absence of therapy.

Design: Cross-sectional genomewide association study.

Methods: We analyzed custom whole exome sequencing and direct human leukocyte antigen (HLA) typing from 202 antiretroviral therapy (ART)-suppressed HIV+ noncontrollers in relation to four measures of the peripheral CD4+ T-cell reservoir: HIV intact DNA, total (t)DNA, unspliced (us)RNA, and RNA/DNA.

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Kidney disease in allogeneic hematopoietic cell transplantation (HCT) recipients is associated with increased mortality rates. BK virus (BKV) viremia has been associated with kidney dysfunction in pediatric HCT recipients; however, few studies have investigated longer-term kidney outcomes in association with BKV in this population. Here we assessed the relationship between BK viremia and changes in estimated glomerular filtration rate (eGFR) in children in the first year post-HCT.

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Importance: Herpes simplex virus type 1 (HSV-1) is the leading cause of first-episode genital herpes in many countries.

Objective: To inform counseling messages regarding genital HSV-1 transmission, oral and genital viral shedding patterns among persons with first-episode genital HSV-1 infection were assessed. The trajectory of the development of HSV-specific antibody and T-cell responses was also characterized.

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Beyond their pulmonary disease, many COVID-19 patients experience a complex constellation of characteristics, including hyperinflammatory responses, autoimmune disorders, and coagulopathies. However, the pathogenesis of these aspects of COVID-19 is obscure. More than 90% of people are latently infected with the lymphotropic herpesviruses Epstein-Barr Virus (EBV) and/or Human Herpesvirus-6 (HHV-6).

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Amplicon-based sequencing methods are central in characterizing the diversity, transmission, and evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), but need to be rigorously assessed for clinical utility. Herein, we validated the Swift Biosciences' SARS-CoV-2 Swift Normalase Amplicon Panels using remnant clinical specimens. High-quality genomes meeting our established library and sequence quality criteria were recovered from positive specimens, with 95% limit of detection of 40.

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BackgroundHerpes simplex virus lymphadenitis (HSVL) is an unusual presentation of HSV reactivation in patients with chronic lymphocytic leukemia (CLL) and is characterized by systemic symptoms and no herpetic lesions. The immune responses during HSVL have not, to our knowledge, been studied.MethodsPeripheral blood and lymph node (LN) samples were obtained from a patient with HSVL.

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Background: Some mutations in the receptor binding domain of the SARS-CoV-2 Spike protein are associated with increased transmission or substantial reductions in vaccine efficacy, including in recently described Omicron subvariants. The changing frequencies of these mutations combined with their differing susceptibility to available therapies have posed significant problems for clinicians and public health professionals.

Objective: To develop an assay capable of rapidly and accurately identifying variants including Omicron in clinical specimens to enable case tracking and/or selection of appropriate clinical treatment.

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Wastewater based epidemiology (WBE) has emerged as a tool to track the spread of SARS-CoV-2. However, sampling at wastewater treatment plants (WWTPs) cannot identify transmission hotspots within a city. Here, we sought to understand the diurnal variations (24 h) in SARS-CoV-2 RNA titers at the neighborhood level, using pump stations that serve vulnerable communities (e.

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Antigen-specific T persist and protect against skin or female reproductive tract (FRT) HSV infection. As the pathogenesis of HSV differs between humans and model organisms, we focus on humans with well-characterized recurrent genital HSV-2 infection. Human CD8+ T persisting at sites of healed human HSV-2 lesions have an activated phenotype but it is unclear if T can be cultivated .

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