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Moreover, the persistence of certain autoantibodies, such as anti-U1-snRNP, anti-SS-B/La, and CHRM3 autoantibodies, in plasma has been linked to specific post-COVID symptoms, including fatigue and dyspnea [83,84]

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FDA approval requires formal clinical trials, safety and efficacy review, labeling approval, and manufacturing validation under a New Drug Application (NDA) or Biologics License Application (BLA)