Studies on allergy and inflammation
dc.contributor.author
Kay, A. B.
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dc.date.accessioned
2018-01-31T11:22:06Z
dc.date.available
2018-01-31T11:22:06Z
dc.date.issued
1979
dc.description.abstract
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dc.description.abstract
The enclosed papers have been classified into five
major sections whose content is as follows:
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dc.description.abstract
SECTION A - The eosinophil leucocyte
The first works are studies on the mechanisms of
eosinophil accumulation following antigen-antibody
(1,2 )
reactions in guinea pig skin. ' y These were extended
to observations on eosinophil chemotaxis in vitro in
relation to the complement system. (3,4)
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dc.description.abstract
The eosinophil chemotactic factor of anaphylaxis
(ECF-A) was first described in 1971.(5,6) Interactions
between ECF-A and complement-derived eosinophilotactic
factors were reported later(7) as were investigations on
the chemical characterisation of ECF-A.(8) Inhibition
of eosinophil chemotaxis by an agent related to disodium
cromoglycate is also described.(9) Other eosinophil
chemotactic agents thought to participate in eosinophil
accumulation in vivo include material derived from
Hodgkin's lymph node cells,histamine and one of its
major catabolites, imidazole acetic acid.(11) The interactions of these agents both in vitro and in vivo were
extensively studied(12,13) and extended to investigations
on the response of eosinophils to an ECF-A tetrapeptide
and histamine in various disease states(14) as well as
the capacity of these agents to mobilise eosinophils in
the skin of atopic and non-atopic human volunteers.(15)
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dc.description.abstract
Evidence was provided that one of the functions of
the eosinophil in allergic tissue reactions may be its
capacity to inhibit mast cell 'regranulation'.(16)
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dc.description.abstract
Membrane receptors for IgG and complement (C4, C3b
and C3d) on human eosinophils and neutrophils and their
relation to eosinophilia were described(17) and this work
led to the observation that the ECF-A tetrapeptides and
histamine both selectively enhance human eosinophil
complement receptors.(18)
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dc.description.abstract
This work, and those of others, was reviewed in
several articles.(19-26)
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dc.description.abstract
SECTION B - Mediators of hypersensitivity
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dc.description.abstract
In 1974 it was shown that both slow reacting substance
of anaphylaxis (SRS-A) and ECF-A were released from
passively sensitized skin following interaction with
specific antigen.(27) The inactivation of SRS-A by the
arylsulphatase contained in various tissues was
described(28`) and later it was shown that appreciable
amounts of human SRS-A were present in lung as a preformed mediator.(29)
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dc.description.abstract
A number of miscellaneous papers relating to
mediators are contained in this section: these include
an observation on complement activation by Corynebacterium
parvum;(30) some chemical and physical properties of
synthetic human fibrinopeptides(31) and the description of
a primate macrophage-cytophilic antibody(32)
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dc.description.abstract
A review of the various biological pathways associated
with the inflammatory response as they relate to complications of blood transfusion were described in a review
article.(33)
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dc.description.abstract
SECTION C - Studies on chemotaxis
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dc.description.abstract
This section contains papers on chemotaxis of
(34)
neutrophils, monocytes and basophils. Particular
attention was given to the identification of chemotactic
agents associated with Hageman factor-dependent path¬
ways(35), fibrin, formation(36,37) and fibrinolysis.(38,39)
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dc.description.abstract
There is a study on the relation between neutrophil
accumulation in vivo and agents that are chemotactic
in vitro.(40)
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dc.description.abstract
Alterations in monocyte chemotaxis in bronchial
carcinoma were described.(41)
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dc.description.abstract
Much of this work, especially the relation between
chemotaxis and haemostasis, was reviewed in 1975.(42)
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SECTION D - Clinical studies
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dc.description.abstract
This section contains reports on alterations in the
complement systems in bronchial asthma(43-45) and the
significance of immunoglobulins and complement in pleural effusions associated with bronchial carcinoma.(46)
Studies on mediators of hypersensitivity in chronic
bronchitis and asthma and their modulation by pharmacological agents are also described.(47,48)
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dc.description.abstract
Detailed immunological investigations of two clinical
cases, one of chronic benign neutropenia(49) and the other
on the effect of transfer factor in chronic mucocutaneous
candidiasis,(50) are described.
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dc.description.abstract
A consideration of how coagulation and other
biological systems may interrelate in the context of
'Stroke' was discussed in a review article.(51)
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dc.description.abstract
SECTION E - Methodology
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dc.description.abstract
This section contains two articles on methodology,
one on the preparation of transfer factor( 52) and the
other on tests of immune function.(53)
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dc.identifier.uri
http://hdl.handle.net/1842/26654
dc.publisher
The University of Edinburgh
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dc.relation.ispartof
Annexe Thesis Digitisation Project 2017 Block 15
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dc.relation.isreferencedby
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dc.title
Studies on allergy and inflammation
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dc.type
Thesis or Dissertation
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dc.type.qualificationlevel
Doctoral
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dc.type.qualificationname
PhD Doctor of Philosophy
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