1.Intestinal Parasitosis in Relation to Anti-Retroviral Therapy, CD4+ T-cell Count and Diarrhea in HIV Patients.
Shehla KHALIL ; Bijay Ranjan MIRDHA ; Sanjeev SINHA ; Ashutosh PANDA ; Yogita SINGH ; Anju JOSEPH ; Manorama DEB
The Korean Journal of Parasitology 2015;53(6):705-712
Intestinal parasitic infections are one of the major causes of diarrhea in human immunodeficiency virus (HIV) seropositive individuals. Antiretroviral therapy has markedly reduced the incidence of many opportunistic infections, but parasite-related diarrhea still remains frequent and often underestimated especially in developing countries. The present hospital-based study was conducted to determine the spectrum of intestinal parasitosis in adult HIV/AIDS (acquired immunodeficiency syndrome) patients with or without diarrhea with the levels of CD4+ T-cell counts. A total of 400 individuals were enrolled and were screened for intestinal parasitosis. Of these study population, 200 were HIV seropositives, and the remaining 200 were HIV uninfected individuals with or without diarrhea. Intestinal parasites were identified by using microscopy as well as PCR assay. A total of 130 (32.5%) out of 400 patients were positive for any kinds of intestinal parasites. The cumulative number of parasite positive patients was 152 due to multiple infections. A significant association of Cryptosporidium (P<0.001) was detected among individuals with CD4+ T-cell counts less than 200 cells/microl.
AIDS-Related Opportunistic Infections/etiology/*immunology/parasitology
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Adult
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Animals
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Anti-HIV Agents/*therapeutic use
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CD4 Lymphocyte Count
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Diarrhea/etiology/*immunology/parasitology
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Female
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HIV Infections/complications/*drug therapy
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Humans
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Intestinal Diseases, Parasitic/etiology/*immunology/parasitology
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Male
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Middle Aged
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Parasites/classification/genetics/*isolation & purification
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Young Adult
2.Gene Therapy for Bone Tissue Engineering.
Young Dong KIM ; Prasad POFALI ; Tae Eun PARK ; Bijay SINGH ; Kihyun CHO ; Sushila MAHARJAN ; Prajakta DANDEKAR ; Ratnesh JAIN ; Yun Jaie CHOI ; Rohidas AROTE ; Chong Su CHO
Tissue Engineering and Regenerative Medicine 2016;13(2):111-125
Gene therapy holds a great promise and has been extensively investigated to improve bone formation and regeneration therapies in bone tissue engineering. A variety of osteogenic genes can be delivered by combining different vectors (viral or non-viral), scaffolds and delivery methodologies. Ex vivo & in vivo gene enhanced tissue engineering approaches have led to successful osteogenic differentiation and bone formation. In this article, we review recent advances of gene therapy-based bone tissue engineering discussing strengths and weaknesses of various strategies as well as general overview of gene therapy.
Bone and Bones*
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Bone Morphogenetic Proteins
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Genetic Therapy*
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Osteogenesis
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Regeneration
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Tissue Engineering
3.Local Delivery of CTGF siRNA with Poly(sorbitol-co-PEI) Reduces Scar Contraction in Cutaneous Wound Healing.
Ki Hyun CHO ; Bijay SINGH ; Sushila MAHARJAN1 ; Yoonjeong JANG ; Yun Jaie CHOI ; Chong Su CHO
Tissue Engineering and Regenerative Medicine 2017;14(3):211-220
Healing process in scarring inevitably produces a considerable amount of non-organized dense collagen-rich matrix called scar thus impairing the native structure of skin. Connective tissue growth factor (CTGF) overexpression within healing tissues is known to play an imperative role in collagen production stimulated by transforming growth factor-beta in cutaneous wound healing. Undoubtedly, the knockdown of CTGF expression through siRNA-mediated gene silencing could simply impede the scarring process. However, the less stability and low transfection of siRNAs themselves urge a safe carrier to protect and transfect them into cells at a high rate avoiding toxicities. Here, we developed a degradable poly(sorbitol-co-PEI) (PSPEI), prepared by polymerization of sorbitol diacrylate with low molecular weight polyethylenimine, which has high transfection efficiency but low cytotoxicity, and utilized it in siCTGF delivery to silence the expression of CTGF in an animal model of cutaneous wound healing. Unlike contracted scar in normal healing, there was no or less contraction in the healed skin of mice treated with siCTGF using PSPEI. Histologically, the healed tissues also had distinct papillary structures and dense irregular connective tissues that were lacking in the control scar tissues. This study exemplifies a successful treatment of cutaneous wound healing using a polymer system coupled with RNA interference. Hence, the approach holds a great promise for developing new treatments with novel targets in regenerative medicines.
Animals
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Cicatrix*
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Collagen
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Connective Tissue
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Connective Tissue Growth Factor
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Gene Silencing
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Mice
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Models, Animal
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Molecular Weight
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Polyethyleneimine
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Polymerization
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Polymers
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Regenerative Medicine
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RNA Interference
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RNA, Small Interfering*
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Skin
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Sorbitol
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Transfection
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Wound Healing*
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Wounds and Injuries*
4.Oral Immunization of FMDV Vaccine Using pH-Sensitive and Mucoadhesive Thiolated Cellulose Acetate Phthalate Microparticles
Ho Bin LEE ; So Yeon YOON ; Bijay SINGH ; Seo Ho OH ; Lianhua CUI ; Changguo YAN ; Sang Kee KANG ; Yun Jaie CHOI ; Chong Su CHO
Tissue Engineering and Regenerative Medicine 2018;15(1):1-11
Several barriers such as gastric pH, enzymatic degradation and rapid transit should be overcome to orally deliver antigens for taking up by epithelial microfold cells in Peyer's patches of small intestine. To solve the above mentioned problems, we designed pH-sensitive and mucoadhesive polymeric microparticles (MPs) prepared by double emulsion technique using cellulose acetate phthalate (CAP) to enhance immune response of foot-and-mouth disease (FMD) virus (FMDV) subunit vaccine. Thiolation of CAP improved mucoadhesive property of CAP to prolong the MPs transit time through the gastrointestinal tract. Thiolated CAP (T-CAP) also slowed down antigen release in acidic pH of stomach but released more antigens in neutral pH of small intestine due to the pH-sensitivity of the T-CAP. Oral immunization of a chimerical multi-epitope recombinant protein as the FMD subunit vaccine via T-CAP MPs effectively delivered the vaccine to Peyer's patches eliciting mucosal IgA response. It will make a step forward into a promising oral subunit vaccine development in livestock industry.
Animals
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Cellulose
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Foot-and-Mouth Disease
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Gastrointestinal Tract
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Hydrogen-Ion Concentration
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Immunization
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Immunoglobulin A
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Intestine, Small
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Livestock
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Peyer's Patches
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Polymers
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Staphylococcal Protein A
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Stomach
5.Ethnopharmacology, phytochemistry and pharmacology of Tephrosia purpurea.
Satadru PALBAG ; Bijay Kr DEY ; Narendra Kumar SINGH
Chinese Journal of Natural Medicines (English Ed.) 2014;12(1):1-7
Tephrosia purpurea (L.) Pers. is popularly known as 'Sarapunkha' in classical Ayurvedic texts. It is a perennial plant belonging to the family Fabaceae, and occurs throughout the Indian subcontinent. T. purpurea is traditionally used to treat splenomegaly, cirrhosis, cough and cold, abdominal swelling and as an antidote in the Ayurvedic system of medicine. Phytochemical investigations indicate the presence of semiglabrin, pongamole, lanceolatins A and B, rutin, lupeol, and β-sitosterol. Flavonoids including (+)-tephrorin A and B, (+)-tephrosone, an isoflavone, 7, 4'-dihydroxy-3', 5'-dimethoxyisoflavone and a chalcone, (+)-tephropurpurin were isolated from the whole plant. Pharmacological activities of different parts of the plant reported include anti-inflammatory, antiulcer, antimicrobial, antioxidant, antiallergic, antidiabetic, hepatoprotective, antitumor and insect repellent activity. In the present review, the literature on the phytochemical and pharmacological investigations of Tephrosia purpurea (L.) Pers. are summarized to August, 2012.
Animals
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Humans
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India
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Medicine, Ayurvedic
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Plant Extracts
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chemistry
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pharmacology
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Tephrosia
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chemistry