Assessing the Role of Anti rh-GAA in Modulating Response to ERT in a Late-Onset Pompe Disease Cohort from the Italian GSDII Study Group.
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Filosto Massimiliano, Cotti Piccinelli Stefano, Ravaglia Sabrina, Servidei Serenella, Moggio Maurizio, Musumeci Olimpia, Donati Maria Alice, Pegoraro Elena, Di Muzio Antonio, Maggi Lorenzo, Tonin Paola, Marrosu Gianni, Sancricca Cristina, Lerario Alberto, Sacchini Michele, Semplicini Claudio, Bozzoni Virginia, Telese Roberta, Bonanno Silvia, Piras Rachele, Maioli Maria Antonietta, Ricci Giulia, Vercelli Liliana, Galvagni Anna, Gallo Cassarino Serena, Caria Filomena, Mongini Tiziana, Siciliano Gabriele, Padovani Alessandro, Toscano Antonio
Аннотация
METHODS: We analyzed clinical findings and performed serial measurements of IgG anti rh-GAA antibody titers from 64 LOPD patients treated with ERT. The first examination (T0) was completed on average at 17.56 months after starting ERT, while the follow-up (T1) was collected on average at 38.5 months. Differences in T0-T1 delta of the six-minute walking test (6MWT), MRC sum score (MRC), gait, stairs and chair performance (GSGC) and forced vital capacity (FVC) were considered and then related to the antibody titers.
RESULTS: Almost 22% of the patients never developed antibodies against GAA, while 78.1% had a positive titer (31.2% patients developed a low titer, 43.8% a medium titer and 3.1% a high titer). No statistical significance was found in relating the T0-T1 delta differences and antibody titers, except for MRC sum score values in a subgroup of patients treated < 36 months, in which those with a null antibody titer showed a greater clinical improvement than patients with a positive titer.
CONCLUSION: Our results confirm that in a large cohort of LOPD patients, anti rh-GAA antibody generation did not significantly affect either clinical outcome or ERT efficacy. However, in the first 36 months of treatment, a possible interference of low-medium antibody titers with the clinical status could be present. Therefore, a careful and regular evaluation of antibody titers, especially in cases with evidence of clinical decline despite ERT, should be performed.