| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
|
|
|
|||||||
|
|||||||||
*
Leukocyte Biology Section, Biomedical Sciences Division, Imperial College School of Medicine, South Kensington, London, United Kingdom; and
Institute of Pharmaceutical Sciences, University of Nottingham, Nottingham, United Kingdom
 |
Abstract |
|---|
 Top Abstract IntroductionMaterials and MethodsResultsDiscussionReferences |
|---|
15 and 50 kDa molecular mass. This activity was specific for
eotaxin, as responses to other agonists tested were unaffected.
Proteolysis of eotaxin was prevented by EDTA and phenanthroline,
indicating that metalloprotease activity was involved. Production of
enzymes inactivating eotaxin may be a strategy employed by helminths to
prevent recruitment and activation of eosinophils at the site of
infection. As such this represents a novel mechanism of regulation of
chemokine function in vivo. The existence of CCR3 ligands other than
eotaxin (e.g., eotaxin-2) may reflect the evolution of host counter
measures to parasite defense systems. |
Introduction |
|---|
|
TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
|---|
The chemokine eotaxin is a potent eosinophil chemoattractant, first described in the bronchoalveolar lavage fluid of allergen-challenged guinea pigs (9, 10). Eotaxin acts through the receptor CCR3, which is expressed on cell types prominent in allergic inflammation, i.e., eosinophils, Th2 cells, mast cells, and basophils (11, 12, 13, 14). Eotaxin acts systemically, in concert with IL-5, to stimulate the release of eosinophils from the bone marrow, and locally, to mediate their selective recruitment to sites of inflammation (15, 16). Disruption of the eotaxin gene in mice suggests that eotaxin is not only an important mediator of eosinophil recruitment during inflammatory responses in the lung, but is also required for maintenance of basal levels of eosinophils in the mucosal tissue of the gut (17, 18).
Parasitic helminths characteristically induce chronic infections that may last for many years, despite the activation of the host immune response apparent in elevated serum IgE concentrations and eosinophilia (19). In vitro, the combination of eosinophils and immune serum is sufficient to activate eosinophils to kill helminth parasites by release of their toxic granule contents. Therefore, to survive, parasites must have evolved mechanisms of resistance to, or down-regulation of host effector functions. The mechanisms used by helminths to evade host immunity may help our understanding of the regulation of Th2-mediated atopic inflammatory diseases such as asthma. Such allergic inflammatory diseases are believed to be caused by the inappropriate response of this arm of the immune system to environmental Ags. Indeed, the inverse correlation between the incidence of allergy and helminth infection in developing populations has led to the suggestion that parasites play important roles in regulating the Th2 response (20).
Hookworms currently infect approximately one-fifth of the human population. They reside in the gut with their mouthparts attached to the mucosal surface, feeding on the released blood, where individual worms may persist for years (21). Hookworms are one of the leading causes of anemia in humans, resulting in retardation of physical and mental development in children when infection intensities are severe. A number of nematode secretions have been described that exhibit potent antiinflammatory activities. For example, neutrophil-inhibitory factor (NIF)3 is a novel class of glycoprotein secreted by Ancylostoma caninum, which exhibits selective and high affinity binding to the integrin CD11b/CD18, an important effector molecule in leukocyte recruitment and activation (22). NIF can block the adhesion of neutrophils to vascular endothelium and their generation of H2O2; and in vivo NIF can prevent neutrophil-dependent lung injury (23). Platelet-activating factor (PAF) is a potent stimulator of eosinophil and neutrophil recruitment and activation, and enhances IgE-mediated killing of helminths by eosinophils (24). The parasite Nippostrongylus braziliensis secretes a PAF acetylhydrolase that cleaves PAF to an inactive form (25).
It is interesting to note that despite apparent activation of peripheral immune responses, localized inflammation is minimal at the site of infection with parasites adapted for the human host, such as Necator americanus, whereas infection with parasites adapted to other hosts, such as Anclyostoma caninum or Anisakis simplex, is associated with pathogenic eosinophilic enteritis (26, 27, 28). We reasoned that helminth parasites may have evolved strategies of immune evasion that target the mediators that recruit eosinophils to the site of infection, thus enabling worm survival in the face of host immunity. In this study, we tested the excretory/secretory products of the hookworm N. americanus for the ability to down-regulate recruitment of eosinophils in response to chemotactic agents.
|
Materials and Methods |
|---|
|
TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
|---|
The excretory/secretory products of adult N. americanus were collected as previously described (29). Briefly, N. americanus was maintained in DSN hamsters (Mesocricetus autatus), by percutaneous infection of neonates with 100 L3 larvae. Adult worms were recovered from the intestines on day 35. Following extensive washing, 30–35 adult worms were incubated for 16 h in 5 ml RPMI containing 2 mM L-glutamine, 100 U/ml penicillin, and 100 µg/ml streptomycin (Life Technologies, Paisley, U.K.). To standardize activity, each batch of NES produced was assessed for fibrinogenolytic protease activity, as previously described, and concentrated so that 20 µl NES digested 10 µg fibrinogen in 4 h (30). Bacterial contamination of NES was absent, as determined by culture of aliquots on L-agar plates and incubation overnight at 37°C.
Protease inhibitors
The following inhibitors of protease activity were used (Sigma, Poole, U.K.) (selectivity in parenthesis): pepstatin A (aspartic proteases), phenanthroline (metalloproteases), trans-epoxysuccinyl-L-leucylamido-(4-guanidino)butane (E-64) (cysteine proteases), PMSF (serine proteases), EDTA (metalloproteases and calcium-dependent proteases), and EGTA (calcium-dependent proteases). Pepstatin A, PMSF, phenanthroline, and E-64 are known to inhibit the four classes of proteases released by N. americanus (30).
In vivo bioassay of 111In-labeled eosinophil accumulation
The recruitment of eosinophils in response to inflammatory mediators in vivo was measured using a skin bioassay, as previously described (31). Briefly, eosinophils were purified from the peritoneal exudate of donor guinea pigs, which had been induced by repeated injection of horse serum. Eosinophils were radiolabeled with 111InCl3 (Amersham Life Science, Little Chalfont, U.K.), and injected i.v. into sedated recipient animals. For each injection site, 60 nM guinea pig eotaxin (generous gift from H. Showell, Pfizer, Groton, CT) or 600 nM leukotriene B4 (LTB4) in 50 µl HBSS was mixed with an equal volume of NES or buffer control, in the presence or absence of protease inhibitors (1 µM pepstatin A, 1 mM phenanthroline, 1 µM E-64, and 0.1 mM PMSF), incubated for 1 h at room temperature, then injected intradermally into the dorsal skin of recipient animals. Injections were performed at duplicate sites on each of four recipient animals per experiment, and the experiment was conducted three times. After 2 h, animals were killed, the dorsal skin removed, the skin injection sites punched out, and 111In-labeled eosinophil accumulation measured using a Cobra gamma counter (Packard Bioscience, Pangbourne, U.K.). Cell recruitment was averaged for the two injection sites on each animal and data expressed as the mean + SEM of the four animals in each group. The statistical significance of the data was analyzed using the Student’s t test.
Eotaxin ELISA
A total of 25 µl NES was mixed with 50 pM guinea pig or human eotaxin (PeproTech, London, U.K.) in the presence or absence of the protease inhibitor cocktail detailed above, in a final volume of 100 µl 0.1% BSA, PBS. After incubation for 1 h at 37°C, 100 µl of protease inhibitor cocktail in PBS was added to all reactions. Immunoreactive eotaxin was measured by specific sandwich ELISAs developed in our laboratories, as previously described (32, 33).
Western blotting of human chemokines
Western blotting was used to assess the time course and specificity of chemokine digestion by NES proteases. A total of 20 pmol of human eotaxin, eotaxin-2, or IL-8 (PeproTech), in 2 µl 0.1% BSA, PBS was mixed with 10 µl of NES and incubated at 37°C. For each chemokine, 20, 10, 5, and 2.5 pmol of chemokine were also incubated in 12 µl PBS to provide a standard curve. The reaction was stopped by the addition of an equal volume of 2x SDS-PAGE sample buffer and immediately boiling for 5 min. Samples were resolved on a 15% SDS-PAGE gel under standard conditions (34). Proteins were transferred onto sequencing grade polyvinylidene difluoride membranes (Millipore, Watford, U.K.) in 25% methanol, 25 mM Tris base, 200 mM glycine, and 1.7 mM SDS for 1 h. Membranes were blocked with 5% fat-free milk powder in PBS for 30 min, followed by incubation overnight at 4°C with primary anti-chemokine Ab at 1:10,000 in 0.1% milk powder in PBS under constant agitation. We used the IgG fraction of rabbit anti-human eotaxin Ab N3, prepared from rabbit serum by precipitation of unwanted proteins with caprylic acid, as described (35, 36). Eotaxin-2 was detected using the mouse anti-human eotaxin-2 Ab 9G6 (generous gift from Dr. Paul Ponath, Leukosite, Cambridge, MA), and IL-8 detected using mouse anti-human IL-8 Ab (R&D Systems, Abingdon, U.K.). Membranes were washed for 3 x 5 min in 0.05% Tween 20, PBS, followed by detection with peroxidase-conjugated secondary Ab at 1:10,000 in 0.1% milk powder in PBS for 1 h at room temperature. Membranes were washed as above and developed using chemiluminescent substrate (Pierce and Warriner, Chester, U.K.) and x-ray film (X-ograph).
Preparation of N. americanus homogenate
Adult worms were homogenized on ice in PBS using a polytron (Kinematica, Lucerne, Switzerland). Insoluble material was removed by centrifugation at 13,000 x g for 10 min and the supernatant retained. Before gel filtration, glycerol was added to the sample to a final concentration of 5%.
S-300HR gel filtration of N. americanus homogenate
Gel filtration was conducted using the low pressure Bio-Rad
(Hemel Hempsted, U.K.) Econosystem. A glass chromatography column (1.5
cm x 50 cm) was packed with Sephacryl S-300 HR and equilbrated
with PBS (flow rate 0.33 ml/min). The column was calibrated and the
void volume determined using broad range gel filtration standards
(200–12.5 kDa; Sigma, Poole, U.K.). A total of 2 ml of adult
homogenate (5 mg protein) was applied to the column, and following
the elution of the void volume, 2-ml fractions were collected and
assayed for their ability to degrade eotaxin.
Measurement of chemokine bioactivity following incubation with homogenate fractions
A total of 25 µl of each fraction was mixed with 75 µl 3 nM eotaxin, eotaxin-2, IL-5 or IL-8, in 0.1% BSA, 10 mM HEPES, PBS, and incubated for 1 h at 37°C to allow digestion to take place. Remaining bioactivity on eosinophils and neutrophils was measured using a FACS-based assay of cell shape change (37). Granulocytes were prepared from the blood of volunteers who were healthy or had asthma, eczema, or hay fever, according to the following technique (under the approval of St Mary’s Hospital Local Ethics Committee). Cells were separated from plasma by centrifugation of citrated whole blood, and the erythrocytes were removed by dextran sedimentation. Monocytic and granulocytic leukocytes were separated over a Histopaque density gradient, and any remaining erythrocytes were removed by hypotonic shock lysis. For the assay, 5 x 105 mixed granulocytes were added to the agonist and incubated at 37°C for 6 min, after which the cells were fixed. A FACScan flow cytometer (Becton Dickinson, Mountain View, CA) was used to separate eosinophils and neutrophils based on their autofluorescence measured in the FL-2 channel. Cell stimulation produces a shape change that is measured as an increase in mean forward scatter, and that is in proportion to the concentration of agonist. Experiments were performed on cells from a minimum of three donors. Using the ANOVA test, the response produced in the presence of each fraction was compared with the response produced by chemokine alone.
Use of selective protease inhibitors to determine the class of protease acting on eotaxin
Eotaxin was incubated with N. americanus gel filtration fractions in the presence of a range of protease inhibitors, to determine the class of protease(s) responsible for chemokine digestion. Following incubation, immunoreactive eotaxin was measured by ELISA. A total of 12.5 µl of each fraction was incubated with 50 pM eotaxin in the presence or absence of protease inhibitors in a final volume of 100 µl 0.1% BSA, PBS. The following inhibitors were used: 20 mM EDTA, 1 mM EGTA, 1 µM pepstatin A, 10 µM E-64, 10 mM phenanthroline, 1 mM PMSF. Controls containing protease inhibitors and eotaxin, but no fraction, were included to ensure that the protease inhibitors did not affect the measurement of eotaxin by the ELISA. Samples were incubated for 1 h at 37°C, followed by cooling on ice and the addition of 150 µl of ice-cold 0.1% BSA, PBS. Eotaxin was measured by ELISA, as described above.
|
Results |
|---|
|
TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
|---|
To determine whether the excretory/secretory products of N.
americanus could inhibit the recruitment of eosinophils in vivo,
we preincubated two mediators of eosinophil recruitment, eotaxin and
LTB4, with NES and measured their activity in an
in vivo bioassay. The chemoattractants were injected intradermally into
recipient guinea pigs, which had previously received radiolabeled
eosinophils i.v. Eosinophil recruitment was determined by counting the
radioactivity at each injection site after 2 h. As shown in Fig. 1
, both eotaxin and
LTB4 stimulated the recruitment of eosinophils to
the site of injection. Preincubation of eotaxin with NES significantly
reduced the recruitment of eosinophils in response to this agonist, but
had no effect on LTB4-mediated recruitment. The
effect of NES on eotaxin could be prevented by the addition of a
cocktail of protease inhibitors (phenanthroline, E-64, pepstatin A, and
PMSF) that has been previously shown to inhibit all classes of protease
activity in NES. The protease inhibitors had no effect on eosinophil
recruitment when injected alone or in combination with
LTB4, and NES did not induce eosinophil
recruitment when injected alone (Fig. 1). Therefore, we conclude that
N. americanus produces proteases that are able to inhibit
eosinophil recruitment in vivo.
|
We investigated the effect of NES on eotaxin immunoreactivity.
Both guinea pig and human eotaxin were incubated with NES in the
presence, or absence, of protease inhibitors and the remaining
immunoreactive chemokine measured by ELISA. As shown in Fig. 2, incubation of both guinea pig and
human eotaxin with NES reduced the eotaxin measurable by ELISA. The
addition of protease inhibitors reversed this, demonstrating that
proteolysis was responsible for the loss of immunoreactivity. The
protease inhibitors themselves had no effect on the ELISA system (data
not shown).
|
Human eotaxin, eotaxin-2, and IL-8 were incubated with NES for 30,
60, or 90 min, and proteolysis was determined using Western blotting.
Following incubation, chemokines were resolved on a 15% acrylamide
SDS-PAGE gel, transferred to a polyvinylidene difluoride membrane, and
detected using specific Abs. For each chemokine, a standard curve was
run on the same gel to show the reduction in signal in proportion to
reducing amounts of chemokine. Eotaxin was rapidly degraded in the
presence of NES (Fig. 3). No eotaxin
degradation products could be detected by the Ab. Under the same
conditions, IL-8 showed no loss of signal even after 90 min of
incubation at 37°C. In a series of three experiments, eotaxin-2
showed no, or very slight, loss of immunoreactivity when incubated with
NES for 90 min. Therefore, N. americanus produces protease
activity that exhibits substrate specificity for eotaxin.
|
To characterize the functional consequences and specificity of
hookworm-derived protease activity further, adult N.
americanus homogenate underwent gel filtration chromatography.
Each fraction was tested for its ability to inhibit chemokine activity
in an in vitro bioassay. Chemokines were preincubated with homogenate
fractions for 1 h at 37°C and then added to mixed granulocytes
that had been freshly isolated from human blood. Bioactive chemokines
produce a shape change in responsive cells that can be measured as an
increase in forward scatter on a flow cytometer (37). We
measured the activity of eotaxin, eotaxin-2, and IL-5 on eosinophils,
and of IL-8 on neutrophils. Fig. 4
shows the activity of each chemokine measured as a change in forward
scatter. Inhibition of eotaxin bioactivity occurred in two major peaks
at fractions 9–12 and 14–17 (p < 0.01, ANOVA
comparison with maximal response), peaking at fractions 11 and 16,
which correspond to molecular mass of 15 and 50 kDa. In contrast,
the same fractions did not significantly alter the shape change
response to IL-8, IL-5, and eotaxin-2, compared with the maximal
response (p > 0.05 in all fractions).
|
N. americanus produces all of the four major classes of
proteases: metallo-, cysteine, aspartic, and serine proteases. To
determine which classes of enzymes were involved in the proteolysis of
eotaxin, we incubated eotaxin with homogenate fractions, in the
presence of individual protease inhibitors. In preliminary experiments,
protease inhibitors were found to interfere with the shape change assay
of eosinophil activation. Therefore, immunoreactive eotaxin was
measured using an ELISA. As shown in Fig. 5, the fractions that show the most
anti-eotaxin activity by ELISA, i.e., fractions 11 and 16, correspond
to those that are the most inhibitory in the bioassay shown in Fig. 4
.
All eotaxin-degrading activity was prevented by the addition of EDTA,
suggesting that the activity was dependent upon divalent cations. Both
peaks of activity were present in EGTA-treated samples, which
selectively chelate calcium, suggesting that the activity is calcium
insensitive. The specific metalloprotease inhibitor, phenanthroline,
inhibited activity in both peaks, suggesting that metalloprotease
activity was responsible for the major activity seen. In addition,
incubation of fractions with the metalloprotease substrate
Suc-Gly-Pro-Leu-Gly-Pro-AMC, indicated that metalloproteases eluted
between fractions 9 and 18, the same region in which eotaxin
degradation occurs (A. B., unpublished data). The aspartyl
protease inhibitor pepstatin A inhibited some activity between these
two peaks (fractions 12–15), suggesting that there may be other
protease activity present that can digest eotaxin, albeit with lower
activity than the major metalloprotease activities seen.
|
|
Discussion |
|---|
|
TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
|---|
We have demonstrated that the adult hookworm N. americanus produces proteases that can cleave eotaxin. Following the action of these proteases, eotaxin can no longer be detected in immunoassays and exhibits no activity on eosinophils in both in vitro assays of eosinophil shape change and in an in vivo assay of eosinophil recruitment. These proteases demonstrate a specificity for eotaxin, as they do not prevent the actions of LTB4, IL-5, or eotaxin-2 on eosinophils or IL-8 on neutrophils. Following gel filtration chromatography of adult worm homogenate, two major peaks of eotaxin-degrading activity were detected. These peaks were inhibited by the addition of EDTA and the specific metalloprotease inhibitor phenanthroline, but not EGTA or any of the other classes of protease inhibitors tested, suggesting that eotaxin is cleaved by calcium-independent metalloproteases. The two peaks of activity may represent two distinct proteases or different molecular mass forms of the same protease, such as glycosylation variants or multimers. The products of Necator are a crude mixture that is known to contain a number of different proteases, with different pH dependencies (30). It will be interesting to discover whether other products of N. americanus exhibit anti-inflammatory properties, under different conditions. Purification of the metalloprotease we describe in this work will allow a fuller characterization of the enzyme’s substrate specificity and biochemistry.
It has long been a puzzle as to how parasites establish chronic infection in the host despite the induction of a strong immune response. To survive, helminth parasites secrete a number of factors that are capable of down-regulating host immune attack. Hookworms secrete NIF, which may block recruitment of inflammatory cells; glutathione-S-transferase, an antioxidant that may neutralize toxic oxygen products of eosinophils; an Igase, which may prevent Ab-mediated immune attack; an acetylcholinesterase, which may inhibit gut contraction; and a hyaluronidase that may facilitate the spreading of these mediators into the surrounding tissue by digesting the extracellular matrix (22, 40, 41, 42, 43). In addition, N. americanus secretions have recently been shown to induce apoptosis in T lymphocytes (44). The activity we describe in this study is likely, therefore, to function in the context of a protective defense shield secreted by the parasite. Helminths have evolved manifold mechanisms of inhibiting various stages of the host attack: cellular recruitment, cell activation, and the actions of toxic cellular products and mediators that induce expulsion of the parasites from the gut (reviewed in Ref. 45). A well-adapted parasite causes morbidity, allowing for chronic production of eggs, rather than mortality, which is likely to occur in a host overburdened with parasite infection or severely immunocompromised. Rather, the parasite and host exist in equilibrium. In reply to the immunosuppressive adaptations of the parasites, the host may evolve new mechanisms of attack. In this respect, it is interesting that the eotaxin-digesting protease activity we describe cannot inactivate eotaxin-2, under the conditions used. Eotaxin-2 has only 39% identical amino acids to eotaxin; however, its activity on eosinophils is indistinguishable from that of eotaxin, signaling selectively via CCR3. It is notable that several different C-C chemokines signal via the same receptor CCR3, for reasons that are unclear. Evolutionary pressure on CCR3 ligands exerted by host defense evasion strategies developed by parasites provides a possible explanation. Proteolysis of eotaxin, as described in this study, may be an example of this phenomenon.
Parasitic helminths secrete a wide range of proteases that play important roles in their life cycles, such as invasion of host tissue and feeding. N. americanus secretes aspartyl, cystenyl, serine, and metalloproteases. These proteases have been found to exhibit fibrinogenolytic and hemoglobinase activity, which would prevent blood clotting at the bite site and facilitate digestion of blood (30, 46). As parasite proteases are often essential for, and unique to the parasitic lifestyle, they represent attractive targets for chemotherapy and vaccine development. For example, vaccination of sheep with a multiprotease-containing complex from the intestine of the nematode Haemonchus contortus results in greatly reduced worm burdens and egg output associated with anti-protease Abs (47). The discovery of proteases that are important virulence factors for parasitic disease may result in the rational design of specific inhibitors as chemotherapeutic agents (48). For example, Schistosoma mansoni secretes a cysteine protease that allows these parasites to digest hemoglobin, a major protein source for their metabolism. Inhibition of cysteine proteases in vivo in murine models of infection resulted in a significant reduction in worm burden, hepatomegaly, and fecundity (49). One precedent for clinical use of protease inhibitors as chemotherapy against infection is in HIV infection, in which they have proved effective at reducing viral levels and delaying the onset of AIDS. In this case, inhibitors are directed against aspartic proteases involved in viral particle assembly. The development of effective agents for treatment of nematode infection is imperative, as these parasites represent major burdens not only on human health, but also financially on agriculture. The antieotaxin proteases we describe in this study are particularly attractive targets for chemotherapy because of their apparent substrate specificity, and may prove to be effective Ags for vaccination against infection.
|
Footnotes |
|---|
2 Address correspondence and reprint requests to Dr. Fiona Culley, Leukocyte Biology Section, Biomedical Sciences Division, Sir Alexander Fleming Building, Imperial College School of Medicine, South Kensington, London, SW7 2AZ, U.K.
3 Abbreviations used in this paper: NIF, neutrophil-inhibitory factor; E-64, trans-epoxysuccinyl-L-leucylamido-(4-guanidino)butane; LTB4, leukotriene B4; NES, Necator americanus excretory/secretory products; PAF, platelet-activating factor.
Received for publication May 5, 2000. Accepted for publication August 29, 2000.
|
References |
|---|
|
TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
|---|
chemokine activity yet lacks sequence homology to known chemokine receptors. Virology 236:316.[Medline]
chemokine receptor. J. Biol. Chem. 269:28539.
and antigen-induced leukocyte accumulation in the guinea pig lung. Am. J. Respir. Cell Mol. Biol. 20:1007.4 and 2 integrin-dependent eosinophil accumulation in rat skin in vivo: delayed generation of eotaxin in response to IL-4. J. Immunol. 160:3569.This article has been cited by other articles:
|
|
 |
|
  Y. Cho, B. F. Jones, J. J. Vermeire, L. Leng, L. DiFedele, L. M. Harrison, H. Xiong, Y.-K. A. Kwong, Y. Chen, R. Bucala, et al. Structural and Functional Characterization of a Secreted Hookworm Macrophage Migration Inhibitory Factor (MIF) That Interacts with the Human MIF Receptor CD74 J. Biol. Chem., August 10, 2007; 282(32): 23447 - 23456. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. Rumbaugh, J. Turchan-Cholewo, D. Galey, C. St. Hillaire, C. Anderson, K. Conant, and A. Nath Interaction of HIV Tat and matrix metalloproteinase in HIV neuropathogenesis: a new host defense mechanism FASEB J, August 1, 2006; 20(10): 1736 - 1738. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 L. Pang, M. Nie, L. Corbett, A. Sutcliffe, and A. J. Knox Mast Cell beta-Tryptase Selectively Cleaves Eotaxin and RANTES and Abrogates Their Eosinophil Chemotactic Activities J. Immunol., March 15, 2006; 176(6): 3788 - 3795. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 A. Leonardi, P. Brun, G. Abatangelo, M. Plebani, and A. G. Secchi Tear Levels and Activity of Matrix Metalloproteinase (MMP)-1 and MMP-9 in Vernal Keratoconjunctivitis Invest. Ophthalmol. Vis. Sci., July 1, 2003; 44(7): 3052 - 3058. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 D. Dagoye, Z. Bekele, K. Woldemichael, H. Nida, M. Yimam, A. Hall, A. J. Venn, J. R. Britton, R. Hubbard, and S. A. Lewis Wheezing, Allergy, and Parasite Infection in Children in Urban and Rural Ethiopia Am. J. Respir. Crit. Care Med., May 15, 2003; 167(10): 1369 - 1373. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 C. Phillips, W. R. Coward, D. I. Pritchard, and C. R. A. Hewitt Basophils express a type 2 cytokine profile on exposure to proteases from helminths and house dust mites J. Leukoc. Biol., January 1, 2003; 73(1): 165 - 171. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. C. M. Paterson, P. Garside, M. W. Kennedy, and C. E. Lawrence Modulation of a Heterologous Immune Response by the Products of Ascaris suum Infect. Immun., November 1, 2002; 70(11): 6058 - 6067. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
V. E. L. Stubbs, P. Schratl, A. Hartnell, T. J. Williams, B. A. Peskar, A. Heinemann, and I. Sabroe Indomethacin Causes Prostaglandin D2-like and Eotaxin-like Selective Responses in Eosinophils and Basophils J. Biol. Chem., July 12, 2002; 277(29): 26012 - 26020. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
K. Watanabe, P. J. Jose, and S. M. Rankin Eotaxin-2 Generation Is Differentially Regulated by Lipopolysaccharide and IL-4 in Monocytes and Macrophages J. Immunol., February 15, 2002; 168(4): 1911 - 1918. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 A. Loukas and P. Prociv Immune Responses in Hookworm Infections Clin. Microbiol. Rev., October 1, 2001; 14(4): 689 - 703. [Abstract] [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
