Role of Cytomegalovirus Replication in Alopecia Areata Pathogenesis

2000 ◽  
Vol 4 (2) ◽  
pp. 63-65 ◽  
Author(s):  
Annamaria Offidani ◽  
Paolo Amerio ◽  
Maria Luisa Bernardini ◽  
Claudio Feliciani ◽  
Guido Bossi

Background: Cytomegalovirus (CMV) infection has been correlated with various autoimmune disorders. Using molecular biology techniques, DNA sequences of CMV have been reported in paraffin sections of alopecia areata (AA) lesions. Reactivation of the CMV infection has been postulated as one of the pathogenic mechanisms in AA. Other studies, using different techniques however have demonstrated no correlation between CMV and AA. Objectives: This study was to clarify the role of CMV infection and to demonstrate the absence of replication of other autoimmune diseases-related herpes virus (EBV) in the pathogenesis of AA. Methods: After extraction of mRNA from tissue samples of a patient with active patchy AA, reverse transcriptase-polymerase chain reaction was carried out using primers specific for some viral members of the β-herpes viridae family (CMV, EBV, HSV). Results: No replication of the CMV or other β-herpes viridae has been detected in any of the samples collected. Conclusions: The results strongly support the hypothesis that CMV is not the triggering factor in AA, neither as a re-activator of the immune response nor as a trigger of the autoimmunity. No other herpes virus is implicated in the pathogenesis of this disease.

RSC Advances ◽  
2016 ◽  
Vol 6 (60) ◽  
pp. 54898-54903 ◽  
Author(s):  
Dalia M. El-Husseini ◽  
Nashwa M. Helmy ◽  
Reham H. Tammam

We experimented the effect of 15 nm unmodified citrate coated GNPs on the key PCR reactants to see if these would enhance the overall outcomes of the reaction. Thus, the optimized GNPs-assisted PCR could be used for more efficient diagnosis of EHV-1.


2018 ◽  
Vol 51 (4) ◽  
pp. 753-758 ◽  
Author(s):  
Sibel Gür ◽  
Nural Erol ◽  
Orhan Yapıcı ◽  
Mehmet Kale ◽  
Mehmet Tolga Tan ◽  
...  

2021 ◽  
Author(s):  
Tahmaseb Jouzdani ◽  
Amir Sadeghi ◽  
Hamed Tahmasbi ◽  
Ramin Shekouhi ◽  
Maryam Sohooli ◽  
...  

Abstract Background Despite years of research, the etiology of achalasia not well understood. Scientists suppose a role for autoimmunity, in this disorder, and probable viral agent, such as herpes virus (HSV). The aim was to find out the frequency of HSV in esophageal muscle samples in patients with achalasia under Heller's myotomy. Methods In this study, 60 patients with achalasia, after fulfilling the consent form, were underwent Heller’s myotomy surgery. Biopsy samples prepared for polymerase chain reaction (PCR) method for HSV DNA detection. After DNA-extraction, replication performed using specific primers. Results The mean age was 40.62 ± 5.08 years. Thirty-nine patients (65%) were female and 21 (35%) were male. Thirty-eight (63.3%) had no history but the else (36.7%) had a positive history of HSV. HSV-1 was positive in three patients (5%). Two females and one male were HSV-positive. Conclusions HSV-1 frequency is not notable among Iranian patients with achalasia. We suggest exploring other viruses, in special that involving the pathogenesis of achalasia, with a larger sample size.


2016 ◽  
Vol 12 (5) ◽  
pp. 3123-3126 ◽  
Author(s):  
Giovanna Carrà ◽  
Cristina Panuzzo ◽  
Sabrina Crivellaro ◽  
Deborah Morena ◽  
Riccardo Taulli ◽  
...  

2017 ◽  
Vol 12 (14) ◽  
pp. 1327-1334 ◽  
Author(s):  
Simone Saintive ◽  
Eliane Abad ◽  
Dennis de C Ferreira ◽  
Mayra Stambovsky ◽  
Fernanda S Cavalcante ◽  
...  

1994 ◽  
Vol 54 (1-2) ◽  
pp. 176
Author(s):  
W. Liedtke ◽  
R. Malessa ◽  
P.M. Faustmann ◽  
K. Schwechheimer ◽  
K. Truebner ◽  
...  

2016 ◽  
Vol 14 (2) ◽  
pp. 115
Author(s):  
Dini Sahfitri Lubis ◽  
Diah Artati

Polymerase chain reaction (PCR) merupakan salah satu metode deteksi cepat koi herpes vrus (KHV). Metode PCR ini sangat sensitif. Sensitivitas tersebut membuatnya dapat digunakan untuk melipatgandakan satu molekul DNA. Konsentrasi dan kualitas DNA dipengaruhi oleh keberhasilan pada saat melakukan ekstraksi DNA. Kegiatan percobaan ini bertujuan untuk mengetahui hasil deteksi virus KHV dengan metode PCR. Keberhasilan analisis PCR sangat dipengaruhi karakteristik DNA genom yang meliputi kemurnian, konsentrasi dan ukuran template. Virus KHV dideteksi menggunakan metode PCR sesuai dengan SNI 7547:2009. Hasil kegiatan deteksi virus KHV menggunakan PCR dari sampel kode I.230–I.286 dapat memvisualisasikan hasil PCR dengan positif KHV dengan ukuran fragmen DNA 290 bp dengan baik. Dapat dilihat dari 57 sampel yang telah diuji memiliki hasil yang berbeda-beda. Hasil uji yang diperoleh yaitu 32 sampel ikan positif terinfeksi KHV dan 25 sampel negatif KHV


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