“…From this viewpoint, the most promising approach is that regarding the production of vaccines based on more conserved antigenic epitopes than the highly variable surfaces of the HA and NA proteins, such as the extracellular portion of the M2 protein, the nucleoprotein and some conserved domains of the HA. 27,[117][118][119] Positive preliminary results for a "universal target" antigen vaccine against influenza have been achieved using the extracellular portion of the M2 protein in the mouse model, in which antibodies elicited by immunization, directed to this domain, have been shown to confer protection against a range of influenza strains: 120 the magnitude of this immune response, in other animal models, remains to be further investigated and the same will be assessed in ongoing clinical trials, with many key-points of this very promising immunization strategy becoming clearer in the near future.…”