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Being ADAPTIVELY immune-
Where did it come from???
Sandeep
Satapathy,
Roll-10079
Innate Immunity
Non pathogen specific Immune
response
Immediate response
No memory of pathogenecity
Both in vertebrates and Lower
Organisms.
Adaptive Immunity
Pathogen specific
Immune response.
Delayed response .
Memory of
pathogenecity.
Only in Higher
Organisms and
Vertebrates.
Hypothesis:
Result
s
Where did the
adaptive molecules
come from?
How spontaneous
is this evolution?
Were there any
precursor cells,which
were initially non-
immune cells?
Mostly the adaptive
immune molecules arose
from the innate molecules
with few exception like
C3,MHC,TdT.
Adaptive molecules evolved
abruptly and isolating their
precursors is tedious.
Molecules with different
alias/function evolved
partly to be immune
molecules while other
retained their identity.
Adaptive molecules/Cells
B Cell Receptors (Ig)
T Cell Receptors(TCR)
Major Histocompatibility
Complex (MHC)
Recombination activation
Gene(RAG)
Terminal dinucleotide
transferases(TdT)
Complement
System
C3,Factor B,Factor
D-Alternative CS-
Innate
MASP-Lectin CS-
Innate
C1,C4,C2-Classical-
Adaptive
Innate Immune System-
Macrophages, NK cells, Nuetrophils,Eosinophils,
Dendritic Cells
Ig(BCR) and TCR Evolution:
Ig and TCRs(have high structural
similarity)- belong to the Ig
superfamily.
RAGS and TdTs- accommodate variability in these
lymphocytic receptors- maximise antigenic determinants
recognition.
Direct ancestors of Igs and TCRs were similar to the Ig
superfamily of NK cells in mammals- Innate precursors
in higher organisms.
Also precursors were similar to Ig superfamily of NITR
family found in invertebrates and bony fish-Innate
precursors in lower organisms.
Horizontal Gene
Transfer
Precursor
of RAG RAG-1&2
Precursor
of TdT
TdTs
No distinct immune
Function
Distinct
lymphocytic
receptor
recombination
MHC Evolution: A short evolutionary dwell
Many diverse group of molecules (classical and non
classical) with both innate and adaptive immune
functions.
These molecules dwindle for different functions
in very short evolutionary timescale.
MHC Class II molecules evolved first from
precursors, like DM genes .
Precursor of MHC II
e.g DM
Involved in antigen
processing
MHC II
Mainly act as chaperons
for antigen presentation.
Complement Cascade
Evolution:
Adaptive
Innate
Non-immune precursors
(Alpha-2-Macroglobulin-
serine protease inhibitor)
(Alternative
CS)
(Classical CS)
Lectin
CS
Conclusion:
Innate Immune molecules
Non-immune cells
Adaptive Immune system
molecules
Dragged force Evolution with few
functionally divergent evolution and
other function and pattern retaining
conserved evolution.
Co-evolution with higher structural
similarity and functional polymorphism.Freque
nt
Rar
e
Both in Lower and higher
organisms.
Only vertebrates and higher
organisms.
Thank you
all..........

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Immuno- evolution: From Innate to adaptive

  • 1. Being ADAPTIVELY immune- Where did it come from??? Sandeep Satapathy, Roll-10079
  • 2. Innate Immunity Non pathogen specific Immune response Immediate response No memory of pathogenecity Both in vertebrates and Lower Organisms. Adaptive Immunity Pathogen specific Immune response. Delayed response . Memory of pathogenecity. Only in Higher Organisms and Vertebrates.
  • 3. Hypothesis: Result s Where did the adaptive molecules come from? How spontaneous is this evolution? Were there any precursor cells,which were initially non- immune cells? Mostly the adaptive immune molecules arose from the innate molecules with few exception like C3,MHC,TdT. Adaptive molecules evolved abruptly and isolating their precursors is tedious. Molecules with different alias/function evolved partly to be immune molecules while other retained their identity.
  • 4. Adaptive molecules/Cells B Cell Receptors (Ig) T Cell Receptors(TCR) Major Histocompatibility Complex (MHC) Recombination activation Gene(RAG) Terminal dinucleotide transferases(TdT) Complement System C3,Factor B,Factor D-Alternative CS- Innate MASP-Lectin CS- Innate C1,C4,C2-Classical- Adaptive Innate Immune System- Macrophages, NK cells, Nuetrophils,Eosinophils, Dendritic Cells
  • 5. Ig(BCR) and TCR Evolution: Ig and TCRs(have high structural similarity)- belong to the Ig superfamily. RAGS and TdTs- accommodate variability in these lymphocytic receptors- maximise antigenic determinants recognition. Direct ancestors of Igs and TCRs were similar to the Ig superfamily of NK cells in mammals- Innate precursors in higher organisms. Also precursors were similar to Ig superfamily of NITR family found in invertebrates and bony fish-Innate precursors in lower organisms.
  • 6. Horizontal Gene Transfer Precursor of RAG RAG-1&2 Precursor of TdT TdTs No distinct immune Function Distinct lymphocytic receptor recombination
  • 7. MHC Evolution: A short evolutionary dwell Many diverse group of molecules (classical and non classical) with both innate and adaptive immune functions. These molecules dwindle for different functions in very short evolutionary timescale. MHC Class II molecules evolved first from precursors, like DM genes . Precursor of MHC II e.g DM Involved in antigen processing MHC II Mainly act as chaperons for antigen presentation.
  • 9. Conclusion: Innate Immune molecules Non-immune cells Adaptive Immune system molecules Dragged force Evolution with few functionally divergent evolution and other function and pattern retaining conserved evolution. Co-evolution with higher structural similarity and functional polymorphism.Freque nt Rar e Both in Lower and higher organisms. Only vertebrates and higher organisms.