Interleukin‐18 serum level before and after intralesional immunotherapy with tuberculin purified protein derivative in patients with cutaneous and genital warts

Background Several studies demonstrated the efficacy of intralesional purified protein derivative (PPD) immunotherapy in warts eradication. Nevertheless, the precise induced immune mechanisms are undetermined. Injected PPD is hypothesized to induce a delayed hypersensitivity reaction associated with...

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Published inJournal of cosmetic dermatology Vol. 21; no. 12; pp. 7035 - 7042
Main Authors Korsa, Hadeer Hazem Abo, Nashaat, Hebat‐Allah Hassan, Halim, Halim Maher, Atwa, Mona A., Mahmoud Marie, Radwa El‐Sayed
Format Journal Article
LanguageEnglish
Published England 01.12.2022
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Abstract Background Several studies demonstrated the efficacy of intralesional purified protein derivative (PPD) immunotherapy in warts eradication. Nevertheless, the precise induced immune mechanisms are undetermined. Injected PPD is hypothesized to induce a delayed hypersensitivity reaction associated with cytokines release. Interleukin (IL)‐18 has a major role in defense against viral infection via inducing interferon‐γ release from T‐helper 1 and natural killer (NK) cells. Moreover, IL‐18 triggers Fas ligand expression on cytotoxic T cells and NK cells enhancing their cytotoxicity against virally infected cells. Aim The aim of this study was to assess the role of IL‐18 in the response to intralesional PPD injection in patients with warts. Methods The study included 25 patients with warts and 25 HCs. Patients underwent PPD skin test, and only patients with positive tests were included and received intralesional PPD injections starting 72 h after the test then every 2 weeks until wart clearance or a maximum of 3 sessions. Serum IL‐18 level was measured via enzyme‐linked immune‐sorbent assay in patients (pre‐treatment and 2 weeks after the last injection) and HCs. Results After 3 sessions of injection, six (24%) patients were designated responders, nine (36%) patients showed partial response, and 10 (40%) patients were designated non‐responders. Serum IL‐18 level, post‐treatment, was significantly higher than pre‐treatment level (p = 0.025) and level in HCs (p = 0.036). Furthermore, the post‐treatment level was significantly higher in responders than non‐responders (p = 0.025). Conclusion IL‐18 is probably implicated in the immune mechanisms induced by PPD injection that cause eradication of warts.
AbstractList Several studies demonstrated the efficacy of intralesional purified protein derivative (PPD) immunotherapy in warts eradication. Nevertheless, the precise induced immune mechanisms are undetermined. Injected PPD is hypothesized to induce a delayed hypersensitivity reaction associated with cytokines release. Interleukin (IL)-18 has a major role in defense against viral infection via inducing interferon-γ release from T-helper 1 and natural killer (NK) cells. Moreover, IL-18 triggers Fas ligand expression on cytotoxic T cells and NK cells enhancing their cytotoxicity against virally infected cells.BACKGROUNDSeveral studies demonstrated the efficacy of intralesional purified protein derivative (PPD) immunotherapy in warts eradication. Nevertheless, the precise induced immune mechanisms are undetermined. Injected PPD is hypothesized to induce a delayed hypersensitivity reaction associated with cytokines release. Interleukin (IL)-18 has a major role in defense against viral infection via inducing interferon-γ release from T-helper 1 and natural killer (NK) cells. Moreover, IL-18 triggers Fas ligand expression on cytotoxic T cells and NK cells enhancing their cytotoxicity against virally infected cells.The aim of this study was to assess the role of IL-18 in the response to intralesional PPD injection in patients with warts.AIMThe aim of this study was to assess the role of IL-18 in the response to intralesional PPD injection in patients with warts.The study included 25 patients with warts and 25 HCs. Patients underwent PPD skin test, and only patients with positive tests were included and received intralesional PPD injections starting 72 h after the test then every 2 weeks until wart clearance or a maximum of 3 sessions. Serum IL-18 level was measured via enzyme-linked immune-sorbent assay in patients (pre-treatment and 2 weeks after the last injection) and HCs.METHODSThe study included 25 patients with warts and 25 HCs. Patients underwent PPD skin test, and only patients with positive tests were included and received intralesional PPD injections starting 72 h after the test then every 2 weeks until wart clearance or a maximum of 3 sessions. Serum IL-18 level was measured via enzyme-linked immune-sorbent assay in patients (pre-treatment and 2 weeks after the last injection) and HCs.After 3 sessions of injection, six (24%) patients were designated responders, nine (36%) patients showed partial response, and 10 (40%) patients were designated non-responders. Serum IL-18 level, post-treatment, was significantly higher than pre-treatment level (p = 0.025) and level in HCs (p = 0.036). Furthermore, the post-treatment level was significantly higher in responders than non-responders (p = 0.025).RESULTSAfter 3 sessions of injection, six (24%) patients were designated responders, nine (36%) patients showed partial response, and 10 (40%) patients were designated non-responders. Serum IL-18 level, post-treatment, was significantly higher than pre-treatment level (p = 0.025) and level in HCs (p = 0.036). Furthermore, the post-treatment level was significantly higher in responders than non-responders (p = 0.025).IL-18 is probably implicated in the immune mechanisms induced by PPD injection that cause eradication of warts.CONCLUSIONIL-18 is probably implicated in the immune mechanisms induced by PPD injection that cause eradication of warts.
Background Several studies demonstrated the efficacy of intralesional purified protein derivative (PPD) immunotherapy in warts eradication. Nevertheless, the precise induced immune mechanisms are undetermined. Injected PPD is hypothesized to induce a delayed hypersensitivity reaction associated with cytokines release. Interleukin (IL)‐18 has a major role in defense against viral infection via inducing interferon‐γ release from T‐helper 1 and natural killer (NK) cells. Moreover, IL‐18 triggers Fas ligand expression on cytotoxic T cells and NK cells enhancing their cytotoxicity against virally infected cells. Aim The aim of this study was to assess the role of IL‐18 in the response to intralesional PPD injection in patients with warts. Methods The study included 25 patients with warts and 25 HCs. Patients underwent PPD skin test, and only patients with positive tests were included and received intralesional PPD injections starting 72 h after the test then every 2 weeks until wart clearance or a maximum of 3 sessions. Serum IL‐18 level was measured via enzyme‐linked immune‐sorbent assay in patients (pre‐treatment and 2 weeks after the last injection) and HCs. Results After 3 sessions of injection, six (24%) patients were designated responders, nine (36%) patients showed partial response, and 10 (40%) patients were designated non‐responders. Serum IL‐18 level, post‐treatment, was significantly higher than pre‐treatment level (p = 0.025) and level in HCs (p = 0.036). Furthermore, the post‐treatment level was significantly higher in responders than non‐responders (p = 0.025). Conclusion IL‐18 is probably implicated in the immune mechanisms induced by PPD injection that cause eradication of warts.
Several studies demonstrated the efficacy of intralesional purified protein derivative (PPD) immunotherapy in warts eradication. Nevertheless, the precise induced immune mechanisms are undetermined. Injected PPD is hypothesized to induce a delayed hypersensitivity reaction associated with cytokines release. Interleukin (IL)-18 has a major role in defense against viral infection via inducing interferon-γ release from T-helper 1 and natural killer (NK) cells. Moreover, IL-18 triggers Fas ligand expression on cytotoxic T cells and NK cells enhancing their cytotoxicity against virally infected cells. The aim of this study was to assess the role of IL-18 in the response to intralesional PPD injection in patients with warts. The study included 25 patients with warts and 25 HCs. Patients underwent PPD skin test, and only patients with positive tests were included and received intralesional PPD injections starting 72 h after the test then every 2 weeks until wart clearance or a maximum of 3 sessions. Serum IL-18 level was measured via enzyme-linked immune-sorbent assay in patients (pre-treatment and 2 weeks after the last injection) and HCs. After 3 sessions of injection, six (24%) patients were designated responders, nine (36%) patients showed partial response, and 10 (40%) patients were designated non-responders. Serum IL-18 level, post-treatment, was significantly higher than pre-treatment level (p = 0.025) and level in HCs (p = 0.036). Furthermore, the post-treatment level was significantly higher in responders than non-responders (p = 0.025). IL-18 is probably implicated in the immune mechanisms induced by PPD injection that cause eradication of warts.
Author Korsa, Hadeer Hazem Abo
Mahmoud Marie, Radwa El‐Sayed
Nashaat, Hebat‐Allah Hassan
Atwa, Mona A.
Halim, Halim Maher
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CitedBy_id crossref_primary_10_3389_fmed_2023_1260139
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Snippet Background Several studies demonstrated the efficacy of intralesional purified protein derivative (PPD) immunotherapy in warts eradication. Nevertheless, the...
Several studies demonstrated the efficacy of intralesional purified protein derivative (PPD) immunotherapy in warts eradication. Nevertheless, the precise...
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SubjectTerms Condylomata Acuminata - chemically induced
Humans
Immunotherapy - adverse effects
infection
Injections, Intralesional
Interleukin-18 - therapeutic use
Interleukin‐18
Treatment Outcome
Tuberculin - adverse effects
viral warts
Warts - drug therapy
Title Interleukin‐18 serum level before and after intralesional immunotherapy with tuberculin purified protein derivative in patients with cutaneous and genital warts
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjocd.15358
https://www.ncbi.nlm.nih.gov/pubmed/36059258
https://www.proquest.com/docview/2709912741
Volume 21
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