Background Vaccination is one of the most significant developments
in modern science, improving the treatment and control-
ling the spread of diseases across communities. For for-
mulation scientists and immunologists, there has been
an interest in the development of liposomal vaccines
for their prophylactic uses in infections (of viral, bacte-
rial, fungal or parasitic origin) [
1
–
3
]. To develop safe and
effective liposome-based vaccines, scientists should take
into consideration several interconnected principles: (1)
the design-dependent function of the liposomes (2) the
characteristics of liposome-cell interactions when vac-
cine administration occurs and (3) the specific cell recep-
tor and signaling involved once liposomal vaccines are
administered. Each of these principles will affect vac-
cine efficacy and its potential development from bench
to bedside applications. These three principles are also
the basis for developing excellent subunit vaccine strat-
egies, which have been of important interest for vaccine
scientists for several years [
4
–
7
]. To comprehend how
the potential liposomal vaccine might work in the host
we must understand the immune responses involved in
receptor signaling. The field of immunology plays a sig-
nificant role that will help determine the utilization of
vaccinology to the advantage of the patient by developing
adequate prophylactic treatment approaches.
Immunologists investigate how our bodies defend
themselves from pathogens by determining and describ-
ing the signaling mechanisms involved. Basically, when
infection occurs, the innate arm of the immune system
responds through recognition of distinct molecules on or
in pathogens termed ‘pathogen associated molecular pat-
terns (PAMPs)’. These PAMPs differ from host markers