1.The Chinese herbal prescription JieZe-1 inhibits caspase-1-dependent pyroptosis induced by herpes simplex virus-2 infection in vitro.
Tong LIU ; Qing-Qing SHAO ; Wen-Jia WANG ; Tian-Li LIU ; Xi-Ming JIN ; Li-Jun XU ; Guang-Ying HUANG ; Zhuo CHEN
Journal of Integrative Medicine 2023;21(3):277-288
OBJECTIVE:
JieZe-1 (JZ-1), a Chinese herbal prescription, has an obvious effect on genital herpes, which is mainly caused by herpes simplex virus type 2 (HSV-2). Our study aimed to address whether HSV-2 induces pyroptosis of VK2/E6E7 cells and to investigate the anti-HSV-2 activity of JZ-1 and the effect of JZ-1 on caspase-1-dependent pyroptosis.
METHODS:
HSV-2-infected VK2/E6E7 cells and culture supernate were harvested at different time points after the infection. Cells were co-treated with HSV-2 and penciclovir (0.078125 mg/mL) or caspase-1 inhibitor VX-765 (24 h pretreatment with 100 μmol/L) or JZ-1 (0.078125-50 mg/mL). Cell counting kit-8 assay and viral load analysis were used to evaluate the antiviral activity of JZ-1. Inflammasome activation and pyroptosis of VK2/E6E7 cells were analyzed using microscopy, Hoechst 33342/propidium iodide staining, lactate dehydrogenase release assay, gene and protein expression, co-immunoprecipitation, immunofluorescence, and enzyme-linked immunosorbent assay.
RESULTS:
HSV-2 induced pyroptosis of VK2/E6E7 cells, with the most significant increase observed 24 h after the infection. JZ-1 effectively inhibited HSV-2 (the 50% inhibitory concentration = 1.709 mg/mL), with the 6.25 mg/mL dose showing the highest efficacy (95.76%). JZ-1 (6.25 mg/mL) suppressed pyroptosis of VK2/E6E7 cells. It downregulated the inflammasome activation and pyroptosis via inhibiting the expression of nucleotide-binding oligomerization domain-like receptor family pyrin domain-containing protein 3 (P < 0.001) and interferon-γ-inducible protein 16 (P < 0.001), and their interactions with apoptosis-associated speck-like protein containing a caspase recruitment domain, and reducing cleaved caspase-1 p20 (P < 0.01), gasdermin D-N (P < 0.01), interleukin (IL)-1β (P < 0.001), and IL-18 levels (P < 0.001).
CONCLUSION
JZ-1 exerts an excellent anti-HSV-2 effect in VK2/E6E7 cells, and it inhibits caspase-1-dependent pyroptosis induced by HSV-2 infection. These data enrich our understanding of the pathologic basis of HSV-2 infection and provide experimental evidence for the anti-HSV-2 activity of JZ-1. Please cite this article as: Liu T, Shao QQ, Wang WJ, Liu TL, Jin XM, Xu LJ, Huang GY, Chen Z. The Chinese herbal prescription JieZe-1 inhibits caspase-1-dependent pyroptosis induced by herpes simplex virus-2 infection in vitro. J Integr Med. 2023; 21(3): 277-288.
Caspase 1/metabolism*
;
Inflammasomes/pharmacology*
;
NLR Family, Pyrin Domain-Containing 3 Protein/metabolism*
;
Pyroptosis
;
Simplexvirus/metabolism*
;
Drugs, Chinese Herbal/pharmacology*
;
Herpes Simplex/drug therapy*
;
Humans
2.Bilateral Acute Retinal Necrosis and Encephalomalacia Due to Herpes Simplex Virus Infection in a Premature Infant
Mi Hye BAE ; Na Rae LEE ; Young Mi HAN ; Lira YOON ; Young Mi KIM ; Shin Yun BYUN ; Jae Jung LEE ; Han Jo KWON ; Min Jung KWAK ; Kyung Hee PARK
Neonatal Medicine 2019;26(1):63-66
Herpes simplex virus (HSV) is a common pathogen, that causes a broad spectrum of diseases, ranging from minor skin infections to severe encephalitis and widespread infections. Acute retinal necrosis (ARN), one of the most serious manifestations of HSV infection, is defined as a rapidly progressing necrotizing retinopathy that presents discrete areas of circumferential retinal necrosis, along with signs of uveitis, vitreitis, and retinal vasculitis. We encountered a case of a female infant, born at 33 weeks of gestation with a body weight at birth of 2,080 g, who had ARN and encephalomalacia due to HSV infection. ARN associated with HSV infection should be suspected when nonspecific retinal exudates are observed in neonates, especially preterm infants.
Body Weight
;
Encephalitis
;
Encephalomalacia
;
Exudates and Transudates
;
Female
;
Herpes Simplex
;
Herpesvirus 2, Human
;
Humans
;
Infant
;
Infant, Newborn
;
Infant, Premature
;
Necrosis
;
Parturition
;
Pregnancy
;
Retinal Necrosis Syndrome, Acute
;
Retinal Vasculitis
;
Retinaldehyde
;
Simplexvirus
;
Skin
;
Uveitis
3.A Case of Corneal Dysplasia with Identification of POLH Gene Variants in Xeroderma Pigmentosum
Eun Hae SHIN ; Dong Hui LIM ; Yoon Duck KIM ; Kyung In WOO ; Jisang HAN ; Jong Eun PARK ; Tae Young CHUNG ; Chang Seok KI
Journal of the Korean Ophthalmological Society 2019;60(4):380-386
PURPOSE: To discuss the clinical course and diagnosis of corneal dysplasia in a xeroderma pigmentosum patient based on a genetic evaluation. CASE SUMMARY: A 42-year-old female visited our clinic for decreased left visual acuity and corneal opacity. She had undergone several surgeries previously due to the presence of basosquamous carcinoma in the left lower eyelid, neurofibroma, and malignant melanoma of the facial skin. The patient showed repeated corneal surface problems, with a suspicious dendritic lesion; however, antiviral therapy was ineffective, and herpes simplex virus polymerase chain reaction results were negative. Despite regular follow-ups, the patient showed neovascularization around the corneal limbus and an irregular corneal surface. We performed corneal debridement with autologous serum eye drops for treatment. The patient's visual acuity and corneal surface improved after the procedure. The impression cytology result was corneal dysplasia. In whole exome sequencing, two pathogenic variants and one likely pathogenic variant of the POLH gene were detected. CONCLUSIONS: This is the first genetically identified xeroderma pigmentosum case with ophthalmological lesions of the eyelid and cornea in Korea. Debridement of the irregular corneal surface and autologous serum eye drop administration in xeroderma pigmentosum could be helpful for improving visual acuity.
Adult
;
Carcinoma, Basosquamous
;
Cornea
;
Corneal Opacity
;
Debridement
;
Diagnosis
;
Exome
;
Eyelids
;
Female
;
Follow-Up Studies
;
Humans
;
Ichthyosis
;
Korea
;
Limbus Corneae
;
Melanoma
;
Neurofibroma
;
Ophthalmic Solutions
;
Polymerase Chain Reaction
;
Simplexvirus
;
Skin
;
Visual Acuity
;
Xeroderma Pigmentosum
4.Chest Pain in a Renal Transplant Recipient due to Concomitant Cytomegalovirus and Herpes Simplex Virus Esophagitis
Seok Hyung KANG ; Myong Ki BAEG ; Sun Hye KO ; Hyunjung HWANG ; Sang Yeop YI ; Sung Jin MOON ; Jeongkeun PARK
The Korean Journal of Helicobacter and Upper Gastrointestinal Research 2019;19(1):61-64
Chest pain in kidney transplant patients is usually caused by cardiac or pulmonary problems. However, it may be rarely caused by opportunistic esophageal infections. A 66-year-old female kidney transplant recipient was admitted because of chest pain. She had been treated with high-dose steroid and immunosuppressants for acute T-cell-mediated rejection. Cardiologic and pulmonary evaluations had normal results. Endoscopic examination revealed three clear ulcerative lesions in the esophagus. Histological and immunohistochemical staining of the endoscopic biopsy specimens revealed coinfection of herpes simplex virus and cytomegalovirus. The patient was treated with intravenous ganciclovir for 2 weeks. Her symptoms completely resolved, and follow-up endoscopy revealed complete healing of the previous ulcers. Viral esophagitis should be considered in the differential diagnosis in kidney transplant recipients presenting with chest pain.
Aged
;
Biopsy
;
Chest Pain
;
Coinfection
;
Cytomegalovirus
;
Diagnosis, Differential
;
Endoscopy
;
Esophagitis
;
Esophagus
;
Female
;
Follow-Up Studies
;
Ganciclovir
;
Herpes Simplex
;
Humans
;
Immunosuppressive Agents
;
Kidney
;
Kidney Transplantation
;
Simplexvirus
;
Thorax
;
Transplant Recipients
;
Ulcer
5.A Case of Chronic Herpes Simplex Virus Infection Misdiagnosed as a Perforating Dermatosis
Korean Journal of Dermatology 2019;57(4):221-222
No abstract available.
Herpes Simplex
;
Simplexvirus
;
Skin Diseases
6.Acute Necrotizing Encephalopathy in Children: a Long Way to Go
Yun Jeong LEE ; Su Kyeong HWANG ; Soonhak KWON
Journal of Korean Medical Science 2019;34(19):e143-
BACKGROUND: Acute necrotizing encephalopathy (ANE) is a rare, but potentially life threatening neurological condition in children. This study aimed to investigate its clinical spectrum, diagnostic and therapeutic dilemma, and prognosis. METHODS: Twelve children with ANE were included in the study. The diagnosis was made by clinical and radiological characteristics from January 1999 to December 2017 and their clinical data were retrospectively analyzed. RESULTS: A total of 12 children aged 6 to 93 months at onset (5 male: 7 female) were evaluated. The etiology was found in 4 of them (influenza A, H1N1; coxsackie A 16; herpes simplex virus; and RANBP2 gene/mycoplasma). The most common initial presentations were seizures (67%) and altered mental status (58%). The majority of the subjects showed elevation of aspartate aminotransferase/alanine aminotransferase with normal ammonia and increased cerebrospinal fluid protein without pleocytosis. Magnetic resonance imaging revealed increased T2 signal density in bilateral thalami in all patients, but the majority of the subjects (67%) also had lesions in other areas including tegmentum and white matter. Despite the aggressive immunomodulatory treatments, the long-term outcome was variable. One child and two sisters with genetic predisposition passed away. CONCLUSION: ANE is a distinctive type of acute encephalopathy with diverse clinical spectrum. Even though the diagnostic criteria are available, they might not be watertight. In addition, treatment options are still limited. Further studies for better outcome are needed.
Ammonia
;
Aspartic Acid
;
Brain Diseases
;
Cerebrospinal Fluid
;
Child
;
Diagnosis
;
Genetic Predisposition to Disease
;
Humans
;
Leukocytosis
;
Magnetic Resonance Imaging
;
Male
;
Prognosis
;
Retrospective Studies
;
Seizures
;
Siblings
;
Simplexvirus
;
White Matter
7.A Case of Eosinophilic Esophagitis Associated with Herpes Esophagitis in a Pediatric Patient
Jisun KIM ; Kunsong LEE ; Wonae LEE
Clinical Endoscopy 2019;52(6):606-611
Eosinophilic esophagitis is a rare disease in Asian countries, but its incidence is growing rapidly in Western countries. The main pathophysiology of eosinophilic esophagitis is esophageal epithelial barrier dysfunction; disruption of the esophageal epithelial barrier easily induces antigen sensitization to foods and aeroallergens, which leads to subsequent esophageal inflammation as a result of eosinophil recruitment. Here we report a case of an 11-year-old Korean boy who suffered from fever, odynophagia, dysphagia, and chest pain. His upper endoscopic findings showed longitudinal ulcers with a volcano-like appearance at the distal esophagus. Polymerase chain reaction test results and biopsy specimens were positive for herpes simplex virus type 1. He was treated with acyclovir and a proton pump inhibitor, but his follow-up endoscopy showed typical patterns of eosinophilic esophagitis, and the biopsy specimens were compatible with the diagnostic criteria for eosinophilic esophagitis. Therefore, we report a very rare case of eosinophilic esophagitis after herpes esophagitis in a Korean child with normal immunity.
Acyclovir
;
Asian Continental Ancestry Group
;
Biopsy
;
Chest Pain
;
Child
;
Deglutition Disorders
;
Endoscopy
;
Eosinophilic Esophagitis
;
Eosinophils
;
Esophagitis
;
Esophagus
;
Fever
;
Follow-Up Studies
;
Herpesvirus 1, Human
;
Humans
;
Incidence
;
Inflammation
;
Male
;
Polymerase Chain Reaction
;
Proton Pumps
;
Rare Diseases
;
Simplexvirus
;
Ulcer
8.Recurrent Kaposi Varicelliform Eruption: Investigation of Clinical Characteristics and Predisposing Factors
Kyung Nam BAE ; Taewook KIM ; Sungmin PARK ; Hyun Joo LEE ; Hyunju JIN ; Hyangsuk YOU ; Woo Haing SHIM ; Gun Wook KIM ; Hoon Soo KIM ; Hyun Chang KO ; Byung Soo KIM ; Moon Bum KIM
Korean Journal of Dermatology 2019;57(9):519-526
BACKGROUND: Kaposi varicelliform eruption (KVE) is a disseminated viral infection primarily caused by the herpes simplex virus in the setting of an underlying chronic skin disease. Few studies have reported the clinical characteristics and predisposing factors for recurrent KVE.OBJECTIVES: To characterize the clinical features and predisposing factors for recurrent KVE.METHODS: This retrospective comparative study of recurrent vs. single-episode KVE was performed at the Pusan National University Hospital between 2004 and 2017.RESULTS: A total of 84 episodes occurred in 60 patients, and of these, 13 patients developed recurrence (21.7%). No statistically significant intergroup difference was observed in the mean age and sex distribution. The face was the most common site of involvement in both groups, followed by the trunk and the upper and lower extremities. Atopic dermatitis was the most common pre-existing disease in both groups; however, Darier's disease was more common in the recurrent KVE group, and this difference was statistically significant. Most patients with KVE (66.7%) showed aggravation of the underlying skin disease within 3 months of KVE onset. This finding was more prominent in patients with recurrent episodes (91.7%) than in those with single-episode KVE (58.3%), (p=0.040).CONCLUSION: This study can contribute to a better understanding of recurrent KVE and guide clinicians in treating patients with conditions predisposing to KVE.
Busan
;
Causality
;
Darier Disease
;
Dermatitis, Atopic
;
Humans
;
Kaposi Varicelliform Eruption
;
Lower Extremity
;
Preexisting Condition Coverage
;
Recurrence
;
Retrospective Studies
;
Sex Distribution
;
Simplexvirus
;
Skin Diseases
9.Successful Treatment of Neonatal Herpes Simplex Infection Presenting as Fulminant Hepatitis with Acyclovir and Peritoneal Dialysis
Seonghye CHOI ; Jang Hoon LEE ; Moon Sung PARK
Neonatal Medicine 2019;26(4):229-232
Disseminated neonatal herpes simplex virus (HSV) infection is a severe disease with a high mortality rate. Here, we report the patient presented with fulminant hepatic failure secondary to HSV infection followed by renal failure without any mucocutaneous symptoms. The patient recovered after treatment with acyclovir and peritoneal dialysis. This is the first known case of a patient in Korea who survived disseminated HSV infection with fulminant liver failure followed by renal failure without undergoing liver transplantation.
Acyclovir
;
Hepatitis
;
Herpes Simplex
;
Humans
;
Infant, Newborn
;
Korea
;
Liver Failure
;
Liver Failure, Acute
;
Liver Transplantation
;
Mortality
;
Peritoneal Dialysis
;
Renal Insufficiency
;
Simplexvirus
10.A Case of Neonatal Meningitis Caused by Streptococcus dysgalactiae subspecies dysgalactiae and Herpes Simplex Virus
Geeyae IM ; Yoonseon PARK ; Minsung KIM ; Ki Hwan KIM ; Sang Yong KIM ; Seung Yun CHUNG
Pediatric Infection & Vaccine 2019;26(3):194-198
Streptococcus dysgalactiae has two main subspecies: S. dysgalactiae subsp. equisimilis (SDSE) and S. dysgalactiae subsp. dysgalactiae (SDSD). SDSE often colonizes and causes infections in humans; however, SDSD is an animal pathogen which often causes pyogenic infection in domestic animals. We present a case of meningitis with SDSD and herpes simplex virus in a 22-day-old newborn baby who had no exposure to animals.
Animals
;
Animals, Domestic
;
Bacteria
;
Colon
;
Herpes Simplex
;
Humans
;
Infant, Newborn
;
Meningitis
;
Simplexvirus
;
Streptococcal Infections
;
Streptococcus

Result Analysis
Print
Save
E-mail