A method of identifying a subject responsive to an administration of 4-aminopyridine or a derivative thereof to prevent, alleviate, or treat a tissue damage or tissue dysfunction caused by an exposure to an infectious pathogen, graft-versus-host disease, sepsis, or any combination thereof,
- wherein the infectious pathogen is capable of causing a severe or critical disruption in a normal tissue function, and
- wherein the method comprises the steps of:
- a) administering to the subject between 1 to 5 therapeutically effective amounts of a pharmaceutical composition comprising a 4-aminopyridine, a derivative of 4-aminopyridine, or a combination thereof;
- b) evaluating the symptoms of the tissue damage or tissue dysfunction caused by exposure to an infectious pathogen capable of causing severe or critical disruptions in normal tissue function, graft-versus-host disease, sepsis, or any combination thereof in a subject in need thereof;
- and
- c) identifying the subject as responsive to 4-aminopyridine administration to prevent, alleviate, or treat the tissue damage or tissue dysfunction caused by the exposure to the infectious pathogen, graft-versus-host disease, sepsis, or any combination thereof when the symptoms of the tissue damage or tissue dysfunction caused by the exposure to the infectious pathogen, graft-versus-host disease, sepsis, or any combination thereof in the subject improved.