A prospective randomized controlled study of Mycobacterium Indicus Pranii vaccine, Measles Mumps Rubella vaccine and Vitamin D3 in extragenital cutaneous warts

被引:2
|
作者
Lahoria, Utkrist [1 ]
Singh, Saurabh [1 ,3 ]
Bhardwaj, Abhishek [1 ]
Budania, Anil [1 ]
Chhajed, Neelam [1 ]
Rajagopal, Srinivasan Varun [1 ]
Singh, Surjit [2 ]
机构
[1] All India Inst Med Sci, Dept Dermatol, Jodhpur, India
[2] All India Inst Med Sci, Dept Pharmacol, Jodhpur, India
[3] All India Inst Med Sci AIIMS, Dept Dermatol, Dermatol OPD, Main OPD Block,AIIMS,Basni Phase 2nd, Jodhpur 342005, Rajasthan, India
关键词
cutaneous warts; immunotherapy; MIP; MMR; vitamin D3; INTRALESIONAL IMMUNOTHERAPY; RECALCITRANT WARTS; W VACCINE; COMMON WARTS; MMR VACCINE; SKIN-TEST; INJECTION; CANDIDA; PALMOPLANTAR; ANTIGENS;
D O I
10.1111/jocd.15564
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
DesignInterventional, prospective, four arm randomized control. SettingOutpatient department, Department of Dermatology, Venereology and Leprology, AIIMS Jodhpur (Rajasthan), India. ParticipantsTwo hundred patients. MethodsThe intervention administered in the groups were normal saline (A), vitamin D-3 (B), MIP (C), and MMR (D). The injections were given into the largest wart at 2-weekly intervals until complete clearance or for a maximum of seven sittings. Post-treatment clearance of the injected wart and the distant wart was compared on the basis of change in wart number, percentage clearance, and mean time to complete clearance. Side effects were recorded. ResultsA total of 197 patients were recruited. The mean percentage improvement in the injected and non-injected warts was 68.4% and 66.8%, respectively. Intention to treat analysis (ITT) showed that complete clearance of lesions in injected wart occurred in placebo, vit D-3, MMR, and MIP arms in 64%, 66%, 58%, and 55% patients, respectively (p > 0.05), while in the non-injected warts in 62%, 64%, 52%, and 53%, respectively (p > 0.05). The mean time to achieve complete clearance of wart was fastest in MIP at 7.1 weeks followed by MMR at 7.2 weeks, VIT D-3 at 7.4 weeks and in placebo group 7.8 weeks (p > 0.05). Side effects noted were fever, pain, erythema, and swelling which was highest in VIT D-3 group (p < 0.05). ConclusionThe efficacy of immunotherapies was comparable to placebo with minimal side effects.
引用
收藏
页码:1400 / 1409
页数:10
相关论文
共 50 条
  • [41] The Immunogenicity and Safety Profile for KM-248, a Combined Measles, Mumps, and Rubella Vaccine, and Its Noninferiority to the Measles Vaccine in Healthy Japanese Children: a Phase 3 Randomized Multicenter Single-Blind Clinical Trial
    Platt, Heather
    Tochihara, Shinji
    Oda, Yoshiaki
    Ueda, Kohji
    JAPANESE JOURNAL OF INFECTIOUS DISEASES, 2021, 74 (05) : 429 - 436
  • [42] Immunogenicity and safety of measles-mumps-rubella vaccine delivered by the aerosol, intradermal and intramuscular routes in previously vaccinated young adults: a randomized controlled trial protocol
    Saha, Sumanta
    Millier, Melanie
    Samaranayaka, Ari
    Edmonds, Liza
    Best, Emma
    Ussher, James
    Anglemyer, Andrew
    Lee, Jennifer
    Tatley, Michael
    Cutts, Felicity
    van Binnendijk, Rob
    Mcintyre, Peter
    PLOS ONE, 2025, 20 (03):
  • [43] Intralesional vitamin D3 versus new topical photodynamic therapy in recalcitrant palmoplanter warts Randomized comparative controlled study
    Ibrahim, Nahla A.
    Fadeel, Doaa A. Abdel
    Sadek, Ahmed
    Fadel, Maha
    Tawfik, Abeer
    PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY, 2020, 32
  • [44] Intralesional Purified Protein Derivative of Tuberculin Versus Intralesional Mycobacterium W Vaccine in Treatment of Recalcitrant Extragenital Warts: A Randomized, Single-Blinded, Comparative Study
    Mohta, Alpana
    Jain, Suresh Kumar
    Mehta, Rajesh Dutt
    Arora, Aakanksha
    INDIAN JOURNAL OF DERMATOLOGY, 2022, 67 (01) : 26 - 30
  • [45] Immunogenicity and safety of the combined vaccine for measles, mumps, and rubella isolated or combined with the varicella component administered at 3-month intervals: randomised study
    dos Santos, Eliane Matos
    Noronha, Tatiana Guimaraes
    Alves, Isabelle Soares
    de Souza Cruz, Robson Leite
    de Vasconcellos Ferroco, Clara Lucy
    Brum, Ricardo Cristiano
    Nunes de Oliveira, Patricia Mouta
    Siqueira, Marilda Mendonca
    Lima, Mariza Cristina
    de Paula Ramos, Francisco Luzio
    Bragagnolo, Camila de Marco
    Bastos Camacho, Luiz Antonio
    de Sousa Maia, Maria de Lourdes
    MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2019, 114
  • [46] Immunogenicity and safety of a second dose of a measles-mumps-rubella vaccine administered to healthy participants 7 years of age or older: A phase III, randomized study
    Abu-Elyazeed, Remon
    Jennings, William
    Severance, Randall
    Noss, Michael
    Caplanusi, Adrian
    Povey, Michael
    Henry, Ouzama
    HUMAN VACCINES & IMMUNOTHERAPEUTICS, 2018, 14 (11) : 2624 - 2631
  • [47] Impact of vitamin D3 supplementation on COVID-19 vaccine response and immunoglobulin G antibodies in deficient women: A randomized controlled trial
    Cesur, Fatih
    Atasever, Zeynep
    Ozoran, Yavuz
    VACCINE, 2023, 41 (17) : 2860 - 2867
  • [48] Immunogenicity and safety of measles-mumps-rubella vaccine delivered by disposable-syringe jet injector in healthy Brazilian infants: A randomized non-inferiority study
    Martins, Reinaldo de Menezes
    Curran, Birute
    Sousa Maia, Maria de Lourdes
    Tavares Ribeiro, Maria das Gracas
    Bastos Camacho, Luiz Antonio
    Freire, Marcos da Silva
    Yoshida Yamamura, Anna Maya
    Siqueira, Marilda Mendonca
    Lemos, Maria Cristina F.
    de Albuquerque, Elizabeth Maciel
    von Doellinger, Vanessa dos Reis
    Homma, Akira
    Saganic, Laura
    Jarrahian, Courtney
    Royals, Michael
    Zehrung, Darin
    CONTEMPORARY CLINICAL TRIALS, 2015, 41 : 1 - 8
  • [49] The immunogenicity and safety of a tetravalent measles-mumps-rubella-varicella vaccine when co-administered with conjugated meningococcal C vaccine to healthy children: A phase IIIb, randomized, multi-center study in Italy
    Durando, Paolo
    Esposito, Susanna
    Bona, Gianni
    Cuccia, Mario
    Desole, Maria Giuseppina
    Ferrera, Giuseppe
    Gabutti, Giovanni
    Pellegrino, Angelo
    Salvini, Filippo
    Henry, Ouzama
    Povey, Michael
    Marchetti, Federico
    VACCINE, 2016, 34 (36) : 4278 - 4284
  • [50] A double-blind, randomized, multicenter, controlled study to evaluate the immunogenicity, safety, and tolerability of varicella vaccine (VARIVAX™) passage extension 34 (PE34) process administered concomitantly with measles, mumps, and rubella vaccine (M-M-R™ II)
    Silas, Peter E.
    Zissman, Edward N.
    Gardner, Julie
    Helian, Shanjun
    Lee, Andrew W.
    Platt, Heather L.
    HUMAN VACCINES & IMMUNOTHERAPEUTICS, 2020, 16 (11) : 2634 - 2640