|
Jose Faro
Received his Ph.D. in Biology
from the University of Santiago de Compostela
(Spain) in 1986. Currently, he is a researcher at the Instituto Gulbenkian
de Ciencia (Oeiras, Portugal), where leads the
Systems Immunology Group.
|
Jose Faro has an interdisciplinary background, being experienced
in laboratory work and in mathematics. He was originally trained
in biology and mathematics at the University of Santiago de Compostela
(USC, Spain). He was a Ph.D. student at the Department of Microbiology
of the USC, where he was trained in immunology, participating in several
projects in immunology of infection (Neisseria meningitidis serogroup
B) and in autoimmunity (NZWxNZB and LPR mice). He developed
in his thesis a theoretical model of the regulation of the immune response
based on the interaction of the idiotypic network with T lymphocytes.
After getting his Ph.D. degree in Biology (1986) he went
to the Department of Immunology, Stockholm University (Sweden), to
do postdoctoral research with Göran Möller (1986-87). There
he used a technique for "decorating" B lymphocytes with monoclonal
antibodies to study B cell activation. Later he moved to Paris to work
with Antonio Coutinho at the Pasteur
Institut (1987-89), where he performed studies on the cells expressing
the Mls a antigen and on the characterization of thymic B lymphocytes.
There he was also involved in the development of techniques to study serum
antibody connectivity. While in Paris, he worked also with the late theoretical
biologist prof. F. Varela at the University of Jussieu-Paris VI, who introduced
him into the field of theoretical immunology. There he started to work in
a mathematical description of the idiotypic network.
In 1990 he moved to the University of Salamanca, where he
started a long-enduring collaborative work with prof. Santiago Velasco,
head of the Applied Physics Unit, on issues that ranged from theoretical
studies in immunology (models of idiotypic network, B cell activation,
thymocyte selection), to studies of predator-prey systems with time
delay, and to development of new experimental methods for pedagogical
demonstrations in the thermodynamics lab. From 1993 to 2000 he was teaching
assistant and instructor of the thermodynamics lab at the Faculty of Physics
(University of Salamanca), and in 2000-2001 he was teacher and lab instructor
of the immunology lab at the Faculty of Pharmacy of the
University of Salamanca.
He is currently engaged in several research programs, notably the modeling
of T and B cell activation, and the development of a combined mathematical/experimental
approach to unravel the physiology of lymphoid follicles (from primary
follicles to germinal center reaction) and the role of hypermutations.
Research Interests
Theoretical and mathematical biology with special focus on dynamical
and organizational issues of the physiology of the immune system,
and their relation to the problems on the extent developmental and adult
animal physiology can be articulated with current evolution theory.
Bridging theorists and experimentalists in specific areas of Biology.
In particular, in respect to the relationship between healthy immune
activity and autoimmune disease.
The organisation of the living and its immediate environmuent and their
mutual, but assymetric, dependency. The possibility to develop a mathematical
language (perhaps based on cathegory theory?) that allows to capture
that organization, and describe the unique properties of biological
entities, complementary to the current mathematical language of physics.
Main Research Project:
Mechanisms involved in the germinal center reaction:
a biomathematical and experimental approach.
Affinity maturation of the humoral immune response and memory B lymphocyte
generation relies on dynamically structured, short-lived organules
so-called germinal centres (GC). Yet, their dynamics is an open problem
in immunology. GCs are derived from primary follicles after Ag-activated
B cells expand in a T cell-dependent fashion at their basal end. GC
B cells undergo extensive proliferation, somatic mutation, massive
cell death and Ag-driven selection, and differentiation into memory
B cells. The present study aims to clarify their rise-and-fall dynamics
by assessing four potential driving mechanisms. A mathematical modelling
strategy is being developed in order to derive experimentally testable
predictions that can discriminate between the different postulated mechanisms.
Selected Publications