Two cases of relapsed HIV-associated visceral leishmaniasis successfully treated with combination therapy
Background The management of visceral leishmaniasis (VL) in HIV-infected patients is often complex with patients experiencing higher mortality rates, more toxic side effects and a higher possibility of treatment failure and relapse than HIV-negative individuals with VL. Case presentation We report o...
Ausführliche Beschreibung
Autor*in: |
Mastroianni, Antonio [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
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2018 |
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Anmerkung: |
© The Author(s) 2018 |
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Übergeordnetes Werk: |
Enthalten in: AIDS research and therapy - London : BioMed Central, 2004, 15(2018), 1 vom: 20. Dez. |
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Übergeordnetes Werk: |
volume:15 ; year:2018 ; number:1 ; day:20 ; month:12 |
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DOI / URN: |
10.1186/s12981-018-0215-x |
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Katalog-ID: |
SPR029205522 |
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520 | |a Background The management of visceral leishmaniasis (VL) in HIV-infected patients is often complex with patients experiencing higher mortality rates, more toxic side effects and a higher possibility of treatment failure and relapse than HIV-negative individuals with VL. Case presentation We report on successful salvage therapy in two HIV-infected patients suffering with disseminated cutaneous and visceral leishmaniasis, recalcitrant to therapy with liposomal amphotericin B. After the employment of combination anti-leishmanial treatment, parasite genomes were not detectable up to the last follow up visit, 57 and 78 weeks after treatment onset, respectively. CD4+ lymphocyte counts fluctuated over time, but were generally higher than counts detected at treatment onset, which likely contributed to protection against VL relapse. Conclusions Results achieved with the anti-leishmanial combination treatment were promising, but are based on only two patients. Future investigation is necessary to confirm the efficacy of this salvage therapy in sustaining the immunological response and control of VL. | ||
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10.1186/s12981-018-0215-x doi (DE-627)SPR029205522 (SPR)s12981-018-0215-x-e DE-627 ger DE-627 rakwb eng Mastroianni, Antonio verfasserin aut Two cases of relapsed HIV-associated visceral leishmaniasis successfully treated with combination therapy 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2018 Background The management of visceral leishmaniasis (VL) in HIV-infected patients is often complex with patients experiencing higher mortality rates, more toxic side effects and a higher possibility of treatment failure and relapse than HIV-negative individuals with VL. Case presentation We report on successful salvage therapy in two HIV-infected patients suffering with disseminated cutaneous and visceral leishmaniasis, recalcitrant to therapy with liposomal amphotericin B. After the employment of combination anti-leishmanial treatment, parasite genomes were not detectable up to the last follow up visit, 57 and 78 weeks after treatment onset, respectively. CD4+ lymphocyte counts fluctuated over time, but were generally higher than counts detected at treatment onset, which likely contributed to protection against VL relapse. Conclusions Results achieved with the anti-leishmanial combination treatment were promising, but are based on only two patients. Future investigation is necessary to confirm the efficacy of this salvage therapy in sustaining the immunological response and control of VL. Opportunistic infection (dpeaa)DE-He213 Protozoal infection (dpeaa)DE-He213 Visceral leishmaniasis (dpeaa)DE-He213 Disseminated cutaneous leishmaniasis (dpeaa)DE-He213 Gaibani, Paolo aut Rossini, Giada aut Vocale, Caterina aut Re, Maria Carla aut Ravaglia, Gianfranco aut Sambri, Vittorio aut Varani, Stefania (orcid)0000-0003-0862-4937 aut Enthalten in AIDS research and therapy London : BioMed Central, 2004 15(2018), 1 vom: 20. Dez. (DE-627)477528538 (DE-600)2173450-1 1742-6405 nnns volume:15 year:2018 number:1 day:20 month:12 https://dx.doi.org/10.1186/s12981-018-0215-x kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2018 1 20 12 |
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10.1186/s12981-018-0215-x doi (DE-627)SPR029205522 (SPR)s12981-018-0215-x-e DE-627 ger DE-627 rakwb eng Mastroianni, Antonio verfasserin aut Two cases of relapsed HIV-associated visceral leishmaniasis successfully treated with combination therapy 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2018 Background The management of visceral leishmaniasis (VL) in HIV-infected patients is often complex with patients experiencing higher mortality rates, more toxic side effects and a higher possibility of treatment failure and relapse than HIV-negative individuals with VL. Case presentation We report on successful salvage therapy in two HIV-infected patients suffering with disseminated cutaneous and visceral leishmaniasis, recalcitrant to therapy with liposomal amphotericin B. After the employment of combination anti-leishmanial treatment, parasite genomes were not detectable up to the last follow up visit, 57 and 78 weeks after treatment onset, respectively. CD4+ lymphocyte counts fluctuated over time, but were generally higher than counts detected at treatment onset, which likely contributed to protection against VL relapse. Conclusions Results achieved with the anti-leishmanial combination treatment were promising, but are based on only two patients. Future investigation is necessary to confirm the efficacy of this salvage therapy in sustaining the immunological response and control of VL. Opportunistic infection (dpeaa)DE-He213 Protozoal infection (dpeaa)DE-He213 Visceral leishmaniasis (dpeaa)DE-He213 Disseminated cutaneous leishmaniasis (dpeaa)DE-He213 Gaibani, Paolo aut Rossini, Giada aut Vocale, Caterina aut Re, Maria Carla aut Ravaglia, Gianfranco aut Sambri, Vittorio aut Varani, Stefania (orcid)0000-0003-0862-4937 aut Enthalten in AIDS research and therapy London : BioMed Central, 2004 15(2018), 1 vom: 20. Dez. (DE-627)477528538 (DE-600)2173450-1 1742-6405 nnns volume:15 year:2018 number:1 day:20 month:12 https://dx.doi.org/10.1186/s12981-018-0215-x kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2018 1 20 12 |
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10.1186/s12981-018-0215-x doi (DE-627)SPR029205522 (SPR)s12981-018-0215-x-e DE-627 ger DE-627 rakwb eng Mastroianni, Antonio verfasserin aut Two cases of relapsed HIV-associated visceral leishmaniasis successfully treated with combination therapy 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2018 Background The management of visceral leishmaniasis (VL) in HIV-infected patients is often complex with patients experiencing higher mortality rates, more toxic side effects and a higher possibility of treatment failure and relapse than HIV-negative individuals with VL. Case presentation We report on successful salvage therapy in two HIV-infected patients suffering with disseminated cutaneous and visceral leishmaniasis, recalcitrant to therapy with liposomal amphotericin B. After the employment of combination anti-leishmanial treatment, parasite genomes were not detectable up to the last follow up visit, 57 and 78 weeks after treatment onset, respectively. CD4+ lymphocyte counts fluctuated over time, but were generally higher than counts detected at treatment onset, which likely contributed to protection against VL relapse. Conclusions Results achieved with the anti-leishmanial combination treatment were promising, but are based on only two patients. Future investigation is necessary to confirm the efficacy of this salvage therapy in sustaining the immunological response and control of VL. Opportunistic infection (dpeaa)DE-He213 Protozoal infection (dpeaa)DE-He213 Visceral leishmaniasis (dpeaa)DE-He213 Disseminated cutaneous leishmaniasis (dpeaa)DE-He213 Gaibani, Paolo aut Rossini, Giada aut Vocale, Caterina aut Re, Maria Carla aut Ravaglia, Gianfranco aut Sambri, Vittorio aut Varani, Stefania (orcid)0000-0003-0862-4937 aut Enthalten in AIDS research and therapy London : BioMed Central, 2004 15(2018), 1 vom: 20. Dez. (DE-627)477528538 (DE-600)2173450-1 1742-6405 nnns volume:15 year:2018 number:1 day:20 month:12 https://dx.doi.org/10.1186/s12981-018-0215-x kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2018 1 20 12 |
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10.1186/s12981-018-0215-x doi (DE-627)SPR029205522 (SPR)s12981-018-0215-x-e DE-627 ger DE-627 rakwb eng Mastroianni, Antonio verfasserin aut Two cases of relapsed HIV-associated visceral leishmaniasis successfully treated with combination therapy 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2018 Background The management of visceral leishmaniasis (VL) in HIV-infected patients is often complex with patients experiencing higher mortality rates, more toxic side effects and a higher possibility of treatment failure and relapse than HIV-negative individuals with VL. Case presentation We report on successful salvage therapy in two HIV-infected patients suffering with disseminated cutaneous and visceral leishmaniasis, recalcitrant to therapy with liposomal amphotericin B. After the employment of combination anti-leishmanial treatment, parasite genomes were not detectable up to the last follow up visit, 57 and 78 weeks after treatment onset, respectively. CD4+ lymphocyte counts fluctuated over time, but were generally higher than counts detected at treatment onset, which likely contributed to protection against VL relapse. Conclusions Results achieved with the anti-leishmanial combination treatment were promising, but are based on only two patients. Future investigation is necessary to confirm the efficacy of this salvage therapy in sustaining the immunological response and control of VL. Opportunistic infection (dpeaa)DE-He213 Protozoal infection (dpeaa)DE-He213 Visceral leishmaniasis (dpeaa)DE-He213 Disseminated cutaneous leishmaniasis (dpeaa)DE-He213 Gaibani, Paolo aut Rossini, Giada aut Vocale, Caterina aut Re, Maria Carla aut Ravaglia, Gianfranco aut Sambri, Vittorio aut Varani, Stefania (orcid)0000-0003-0862-4937 aut Enthalten in AIDS research and therapy London : BioMed Central, 2004 15(2018), 1 vom: 20. Dez. (DE-627)477528538 (DE-600)2173450-1 1742-6405 nnns volume:15 year:2018 number:1 day:20 month:12 https://dx.doi.org/10.1186/s12981-018-0215-x kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2018 1 20 12 |
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10.1186/s12981-018-0215-x doi (DE-627)SPR029205522 (SPR)s12981-018-0215-x-e DE-627 ger DE-627 rakwb eng Mastroianni, Antonio verfasserin aut Two cases of relapsed HIV-associated visceral leishmaniasis successfully treated with combination therapy 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2018 Background The management of visceral leishmaniasis (VL) in HIV-infected patients is often complex with patients experiencing higher mortality rates, more toxic side effects and a higher possibility of treatment failure and relapse than HIV-negative individuals with VL. Case presentation We report on successful salvage therapy in two HIV-infected patients suffering with disseminated cutaneous and visceral leishmaniasis, recalcitrant to therapy with liposomal amphotericin B. After the employment of combination anti-leishmanial treatment, parasite genomes were not detectable up to the last follow up visit, 57 and 78 weeks after treatment onset, respectively. CD4+ lymphocyte counts fluctuated over time, but were generally higher than counts detected at treatment onset, which likely contributed to protection against VL relapse. Conclusions Results achieved with the anti-leishmanial combination treatment were promising, but are based on only two patients. Future investigation is necessary to confirm the efficacy of this salvage therapy in sustaining the immunological response and control of VL. Opportunistic infection (dpeaa)DE-He213 Protozoal infection (dpeaa)DE-He213 Visceral leishmaniasis (dpeaa)DE-He213 Disseminated cutaneous leishmaniasis (dpeaa)DE-He213 Gaibani, Paolo aut Rossini, Giada aut Vocale, Caterina aut Re, Maria Carla aut Ravaglia, Gianfranco aut Sambri, Vittorio aut Varani, Stefania (orcid)0000-0003-0862-4937 aut Enthalten in AIDS research and therapy London : BioMed Central, 2004 15(2018), 1 vom: 20. Dez. (DE-627)477528538 (DE-600)2173450-1 1742-6405 nnns volume:15 year:2018 number:1 day:20 month:12 https://dx.doi.org/10.1186/s12981-018-0215-x kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2018 1 20 12 |
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Enthalten in AIDS research and therapy 15(2018), 1 vom: 20. Dez. volume:15 year:2018 number:1 day:20 month:12 |
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Mastroianni, Antonio misc Opportunistic infection misc Protozoal infection misc Visceral leishmaniasis misc Disseminated cutaneous leishmaniasis Two cases of relapsed HIV-associated visceral leishmaniasis successfully treated with combination therapy |
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Two cases of relapsed HIV-associated visceral leishmaniasis successfully treated with combination therapy Opportunistic infection (dpeaa)DE-He213 Protozoal infection (dpeaa)DE-He213 Visceral leishmaniasis (dpeaa)DE-He213 Disseminated cutaneous leishmaniasis (dpeaa)DE-He213 |
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two cases of relapsed hiv-associated visceral leishmaniasis successfully treated with combination therapy |
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Two cases of relapsed HIV-associated visceral leishmaniasis successfully treated with combination therapy |
abstract |
Background The management of visceral leishmaniasis (VL) in HIV-infected patients is often complex with patients experiencing higher mortality rates, more toxic side effects and a higher possibility of treatment failure and relapse than HIV-negative individuals with VL. Case presentation We report on successful salvage therapy in two HIV-infected patients suffering with disseminated cutaneous and visceral leishmaniasis, recalcitrant to therapy with liposomal amphotericin B. After the employment of combination anti-leishmanial treatment, parasite genomes were not detectable up to the last follow up visit, 57 and 78 weeks after treatment onset, respectively. CD4+ lymphocyte counts fluctuated over time, but were generally higher than counts detected at treatment onset, which likely contributed to protection against VL relapse. Conclusions Results achieved with the anti-leishmanial combination treatment were promising, but are based on only two patients. Future investigation is necessary to confirm the efficacy of this salvage therapy in sustaining the immunological response and control of VL. © The Author(s) 2018 |
abstractGer |
Background The management of visceral leishmaniasis (VL) in HIV-infected patients is often complex with patients experiencing higher mortality rates, more toxic side effects and a higher possibility of treatment failure and relapse than HIV-negative individuals with VL. Case presentation We report on successful salvage therapy in two HIV-infected patients suffering with disseminated cutaneous and visceral leishmaniasis, recalcitrant to therapy with liposomal amphotericin B. After the employment of combination anti-leishmanial treatment, parasite genomes were not detectable up to the last follow up visit, 57 and 78 weeks after treatment onset, respectively. CD4+ lymphocyte counts fluctuated over time, but were generally higher than counts detected at treatment onset, which likely contributed to protection against VL relapse. Conclusions Results achieved with the anti-leishmanial combination treatment were promising, but are based on only two patients. Future investigation is necessary to confirm the efficacy of this salvage therapy in sustaining the immunological response and control of VL. © The Author(s) 2018 |
abstract_unstemmed |
Background The management of visceral leishmaniasis (VL) in HIV-infected patients is often complex with patients experiencing higher mortality rates, more toxic side effects and a higher possibility of treatment failure and relapse than HIV-negative individuals with VL. Case presentation We report on successful salvage therapy in two HIV-infected patients suffering with disseminated cutaneous and visceral leishmaniasis, recalcitrant to therapy with liposomal amphotericin B. After the employment of combination anti-leishmanial treatment, parasite genomes were not detectable up to the last follow up visit, 57 and 78 weeks after treatment onset, respectively. CD4+ lymphocyte counts fluctuated over time, but were generally higher than counts detected at treatment onset, which likely contributed to protection against VL relapse. Conclusions Results achieved with the anti-leishmanial combination treatment were promising, but are based on only two patients. Future investigation is necessary to confirm the efficacy of this salvage therapy in sustaining the immunological response and control of VL. © The Author(s) 2018 |
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Two cases of relapsed HIV-associated visceral leishmaniasis successfully treated with combination therapy |
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