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Prepublished online as a Blood First Edition Paper on October 24, 2002; DOI 10.1182/blood-2002-09-2840.
CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS
From the Divisions of Hematology and Clinical
Immunology, Department of Medicine, Mount Sinai School of Medicine, New
York, NY.
Leukocyte adhesion deficiency type 2 (LADII) is characterized
by defective selectin ligand formation, recurrent infection, and mental
retardation. This rare syndrome has only been described in 2 kindreds
of Middle Eastern descent who have differentially responded to
exogenous fucose treatment. The molecular defect was recently ascribed
to single and distinct missense mutations in a putative Golgi
guanosine diphosphate (GDP)-fucose transporter. Here, we describe
a patient of Brazilian origin with features of LADII. Sequencing of the
GDP-fucose transporter revealed a novel single nucleotide deletion
producing a shift in the open-reading frame and severe truncation of
the polypeptide. Overexpression of the mutant protein in the patient's
fibroblasts did not rescue fucosylation, suggesting that the deletion
ablated the activity of the transporter. Administration of oral
L-fucose to the patient produced molecular and clinical responses, as
measured by the appearance of selectin ligands, normalization of
neutrophil counts, and prevention of infectious recurrence. The lower
neutrophil counts paralleled improved neutrophil interactions with
activated endothelium in cremasteric venules of nonobese
diabetic/severe combined immunodeficiency (NOD/SCID) mice. However,
fucose supplementation induced autoimmune neutropenia and the
appearance of H antigen on erythrocytes, albeit without evidence of
intravascular hemolysis. The robust response to fucose despite a
severely truncated transporter suggests alternative means to transport
GDP-fucose into the Golgi complex.
(Blood. 2003;101:1705-1712) The interactions of neutrophils with endothelial
cells that line the blood vessels are necessary for their migration to
sites of inflammation. This dynamic process follows a multistep
sequence that is initiated by initial tethering and rolling mediated by P- and E-selectins expressed on activated venules and their
glycoconjugated ligands on leukocytes.1-3
Selectin ligands undergo several key posttranslational modifications
for selectin binding, including sialylation, fucosylation, and tyrosine
or carbohydrate sulfation.4,5 In particular, the addition
of fucose to O-linked glycan structures was shown to be
critical for selectin recognition because mice deficient in the
leukocyte fucosyltransferases IV and VII display leukocyte adhesion
defects that parallel those found in selectin-deficient mice.6-8 The importance of fucosylation in
selectin-mediated interactions is further evidenced with the
description of a rare leukocyte adhesion deficiency (LAD) syndrome
characterized by a systemic defect in fucose metabolism.9
Patients with LAD syndromes have marked leukocytosis and recurrent
infections without pus formation.10 In contrast to LAD
type 1 (LADI), in which the function or expression of The gene defective in LADII was recently cloned and was found to encode
a putative guanosine diphosphate (GDP)-fucose transporter predicted to
span the Golgi membrane 10 times.21,22 Single and distinct
missense mutations were identified in Arab and Turkish kindred, thus
providing a molecular explanation for the differential response to
fucose. In the present report, we describe a new manifestation of LADII
in a patient of Brazilian origin and no known Middle Eastern descent.
The disease in this patient stems from a novel single nucleotide
deletion leading to frameshift and premature arrest in the translation
of the GDP-fucose transporter gene. We show that this patient responds
well to fucose therapy and that partial restoration of P-selectin
ligand function on the patient's neutrophils correlates with an
increased ability to roll in cremasteric venules of immunodeficient
nonobese diabetic/severe combined immunodeficiency (NOD/SCID) mice. We
further demonstrate that the induction of fucosylated conjugates leads
to the expression of the H antigen on erythrocytes and the production
of antineutrophil antibodies.
Antibodies, reagents, and fucose administration
Mice
Isolation of neutrophils Neutrophils were purified from anticoagulated venous blood samples from the LADII patient or from healthy adult volunteers in a Histopaque1119 (1.119 g/mL; Sigma Diagnostics, St Louis, MO) and Ficoll-Paque (1.077 g/mL; Amersham Pharmacia Biotec, Uppsala, Sweden) discontinuous gradient, and they were washed in phosphate-buffered saline (PBS) containing 2 mM EDTA (ethylenediaminetetraacetic acid) and 0.5% bovine serum albumin (BSA) (PEB buffer). For intravital microscopy experiments, purified human neutrophils were fluorescently labeled by incubation with 33 µM carboxyfluorescein succinimidyl ester (CFSE; Molecular Probes, Eugene, OR) for 30 minutes at 6°C and were washed 3 times in RPMI 1640 before injection into mice through a carotid artery catheter. Human blood samples were obtained in accordance with protocols approved by the Internal Review Board of Mount Sinai School of Medicine.Antineutrophil antibody and H antigen assays Antineutrophil antibody activity in the patient's serum was detected by flow cytometry. Purified neutrophils from healthy donors were incubated with a 1:100 dilution of sera obtained from the peripheral blood of healthy donors or the LADII patient, washed, and further incubated with Cy5-conjugated antihuman IgG antibody. After a final wash, cells were analyzed on a FACScalibur flow cytometer (Becton Dickinson, Mountain View, CA) or were subjected to cytospin and prepared for fluorescence microscopy. Granulocyte agglutination (GA) and monoclonal antibody-specific immobilization of neutrophil antigens (MAIGA) assays were also performed in parallel (Neutrophil Serology Laboratory; American Red Cross, St Paul, MN) using a panel of donor neutrophils serologically phenotyped for the NA1, NA2, NB1, NB2, 5A, 5B, 9A, and MART antigens. Neutrophils were incubated with patient serum and monoclonal antibodies specific for these epitopes. GA was graded subjectively, and MAIGA was graded by enzyme-linked immunosorbent assay (ELISA). Titers were measured using doubling dilutions in the GA assays. Red blood cell agglutination with anti-A, anti-B, anti-A/B, and anti-H was examined according to standard blood bank procedures (Mount Sinai Medical Center and New York Blood Center). H antigens on the patient's RBCs were detected with polyclonal anti-H antibodies from human Bombay donors and the -linked, fucose-specific
lectin A aurantia.
Cell culture and generation of the lymphoblastoid cell line Fibroblasts were obtained through skin biopsy of the LADII patient and were cultured in Dulbecco modified Eagle medium (DMEM; CellGro, Herndon, VA) containing 10% fetal calf serum (FCS; Hyclone, Logan, UT) and antibiotics. For the generation of a lymphoblastoid cell line, low-density mononuclear cells (MNCs) were collected after centrifugation at 250g over Ficoll-Paque of a blood sample from the LADII patient. B-lymphoid cells were transformed and selected by plating MNCs in 10 mL RPMI 1640 plus 10% FCS, also containing 2 µg/mL cyclosporin A (CSA; Novartis Pharmaceutical, East Hanover, NJ), 10 µg/mL phytohemagglutinin (Gibco, Grand Island, NY), and 1 mL Epstein-Barr virus (EBV) supernatant. After 10 days of culture, lymphoid colonies were expanded and selected in RPMI plus 10% FCS containing 2 µg/mL CSA. The transformed LADII-derived lymphoid cell line was further cultured in RMPI plus 10% FCS and antibiotics. The B7 EBV-transformed lymphoblastoid cell line established from a healthy donor (generous gift of Yande Kuang, Mount Sinai School of Medicine, NY) was used as control. All cultures were performed at 37°C and 5% CO2 atmosphere.Flow cytometry and selectin chimera binding assay Cells were washed in PEB buffer before incubation with 15 µg/mL biotinylated A aurantia lectin or 10 µg/mL primary antibodies. After washing in PEB buffer, the cells were incubated with a 1:100 dilution of fluorescein isothiocyanate (FITC)-conjugated streptavidin or Cy5-conjugated antirat antibody (both from Jackson Immunoresearch, West Grove, PA). After a final wash, cells were analyzed by flow cytometry. All incubations were performed for 15 minutes at 6°C.Selectin chimera binding assays were performed as described.23 Briefly, neutrophils were incubated for 15 minutes at 6°C in staining buffer (RPMI containing 5% FCS and 0.05% NaN3) containing a human P-selectin IgG that had been preconjugated to biotinylated Protein A or with the supernatant of COS-7 cells transfected with the murine E-selectin IgM chimera vector. Selectin binding was detected by incubation with an excess of FITC-conjugated streptavidin (1.5 µg) or an FITC-conjugated antihuman IgM antibody (1:50 dilution; Jackson Immunoresearch). Cells were washed in staining buffer and analyzed by flow cytometry. In control samples, the staining was carried out in the presence of 5 mM EDTA. cDNA cloning and sequencing mRNA was isolated from the healthy B7 or the LADII-derived DF1 lymphoblastoid cell lines using the Trizol reagent (Life Technologies), and cDNA was prepared using the ThermoScrip reverse transcription-polymerase chain reaction (RT-PCR) system (Invitrogen, Carlsbad, CA) as indicated by the manufacturer. The putative GDP-fucose transporter (GDP-FucTP) cDNA (encompassing the entire coding region) was amplified by PCR using the high-fidelity Platinum Taq polymerase (Invitrogen) and the following primers: forward ORF-F, 5'-GATCCTGCACATGGCGCTGA-3'; reverse ORF-R, 5'-AGTAGCACCCAGTCCACACC-3'. PCR was performed as follows: 94°C for 5 minutes followed by 35 cycles of 94°C for 30 seconds, 68°C for 30 seconds, and 72°C for 1.5 minutes, and a final extension at 72°C for 7 minutes. PCR products were subcloned into the Zero Blunt TOPO TA PCR cloning system (Invitrogen) and finally cloned for expression in the bicistronic pIRES-hrGFP-1a vector (Stratagene). Sequencing of the GDP-FucTP gene was performed using ORF-F and ORF-R as external primers and ORF-2F (5'-TCAACGCCATCTACACCACGA-3') and ORF-2R (5'-CGTTGTTGTAGAAAGTCA-3') as internal primers, using an ABI Prism 3700 automatic DNA analyzer (DNA sequencing core facility; Mount Sinai School of Medicine). For sequencing of genomic DNA, total cell DNA was extracted from the DF1 cell line and skin fibroblasts (both of patient's origin) or MNCs from both the mother and the father, and the 2 exons of the GDP-FucTP gene were amplified by PCR using the following primers: exon 1 (forward, 5'-GGGCTGCGGCTTCCTT-3'; reverse, TCCCCATGACCACTCTATCC-3') and exon 2 (forward, 5'-TCACCCTTCCCCACTCCTCCTCTC-3'; reverse, 5'-GTAGCACCCAGTCCACACCACAGC-3'). PCR was performed as follows: 94°C for 3 minutes followed by 35 cycles of 94°C for 30 seconds, 59.5°C (for exon 1) or 63.3°C (for exon 2) for 30 seconds, and 72°C for 1 minute, and a final extension at 72°C for 7 minutes. The same sets of primers were used for sequencing. Sequencing data were analyzed using the Sequencher Software (Genes Codes, Ann Arbor, MI).Complementation assays Skin fibroblasts derived from the LADII patient were transfected by electroporation (960 µF, 280 V) with the pIRES-hrGFP-1a vector (Stratagene, La Jolla, CA) containing the GDP-fucose transporter cDNA obtained from either the LADII or healthy lymphoblastoid cell lines. After 48 hours, transfected fibroblasts were plated on coverslips for 1 week. Cells were washed, fixed in 3.7% formaldehyde, and permeabilized with 0.1% Triton X100 (Fischer Scientific) in PBS. Cells were then stained with biotinylated AAL (2 µg/mL) in PEB, washed extensively, and incubated in a solution containing a 1:500 dilution of Cy5-conjugated streptavidin (Jackson Immunoresearch) in PEB. After a final wash, coverslips containing the stained cells were mounted on slides using Vectashield (Vector Laboratories, Burlingame, CA). All incubations were performed for 20 minutes at room temperature. Specificity of the staining with AAL was determined in preliminary experiments in which lectin binding to COS-7 cells could be completely blocked by the presence of 100 mM L-fucose in the staining solution and by the absence of AAL staining in nontransfected LADII fibroblasts. Samples were analyzed under a fluorescence microscope (Zeiss Axiophot 2; Zeiss Axiophot, Thornwood, NY), and images were acquired with an Orca-100 charge-coupled device (CCD) camera (Hamamatsu, Hamamatsu City, Japan) and analyzed with the OpenLab image software.Intravital microscopy experiments NOD/SCID animals were prepared for intravital microscopy of the cremaster muscle as previously described.24 Before the exteriorization of the cremaster muscle, the trachea was cannulated to allow spontaneous respiration, and a PE-10 catheter (Becton Dickinson) was inserted into the common left carotid artery to allow the injection of labeled cells. In some experiments, 107 nonlabeled human MNCs from each sample were injected immediately before the injection of labeled neutrophils to block potential sites of retention of human cells. CFSE-labeled neutrophils (5-20 × 106 cells) collected from the patient at different times of treatment, or from untreated healthy volunteers, were injected, and the cremasteric venules were visualized with an intravital microscope (MM-40; Nikon, Tokyo, Japan) equipped with a mercury fluorescence lamp and water immersion 10 × objective (Nikon; NA 0.3, water). Images were captured using an SIT camera (Hamamatsu) and a camera-controller (C2400; Hamamatsu) and were recorded using an S-VHS video recorder (SV0-9500MD; Sony, San Jose, CA). For analysis of the intravital experiments, hemodynamic parameters and numbers of rolling cells were calculated as described previously.23Statistical analysis All values are reported as mean ± SEM. Statistical significance was analyzed using the Student t test.
New case of LADII A 7-month-old boy of consanguineous Brazilian descent with microcephaly, multiple choroid plexus cysts, hypospadias, bilateral hydronephrosis, and developmental delay was examined for evaluation of recurrent infections, including 4 hospitalizations for fever, gastroenteritis, and severe cellulitis. There was no history of immunodeficiency in the family. Total white blood cell counts ranged from 30 000 to 83 000 cells/mL and absolute neutrophil counts from 6000 to 56 000 cells/mL. Fever episodes rapidly responded to antibiotic therapy, and blood cultures were always sterile. Immunologic evaluation of T-cell numbers and function, immunoglobulin levels, and CD11/18 expression were all within normal range. LADII was diagnosed by the absence of the sialyl Lewis X (sLeX) antigen, impaired E- and P-selectin binding, and presence of the Bombay blood type.Cloning of the GDP-fucose transporter gene reveals a single-base deletion before the sixth transmembrane domain The gene responsible for the LADII syndrome has been recently shown to encode a putative Golgi GDP-fucose transporter whose structure predicts 10 transmembrane domains. Sequencing of the GDP-fucose transporter from the genome of the 2 known families of LADII revealed single and distinct missense mutations. The Turkish patient had a C>T transition at base 439, which led to the substitution of an arginine for a cysteine (Arg147Cys) in the fourth transmembrane domain. Three Arab patients exhibited a 923C>G transversion that replaced threonine for arginine (Thr308Arg) in the ninth transmembrane domain.21,22,25 To sequence the GDP-FucTP gene, we established an Epstein-Barr virus (EBV)-transformed cell line (DF1) from the patient's peripheral B cells. Full-length cDNA from the GDP-FucTP gene was amplified by RT-PCR and was subcloned into a bicistronic expression vector containing the GFP gene after the internal ribosomal entry site (IRES) sequence. Wild-type GDP-FucTP was cloned from a lymphoblastoid line (B7) derived from a control subject and was subcloned into the same vector. The size and amount of GDP-FucTP mRNA expressed in DF1 were roughly similar to those of the control cell line, suggesting that the overall integrity of the patient's GDP-FucTP gene was preserved (data not shown). Sequencing of 2 independent subclones of GDP-FucTP from DF1 revealed a single nucleotide deletion at position 588 ( G588), whereas the sequence of the wild-type GDP-FucTP was
consistent with that published.21,22 To further confirm
these results, we sequenced amplicons from each of the 2 GDP-FucTP
exons obtained from DNA extracts of the LADII DF1 cell line and primary
skin fibroblasts and from the parent's peripheral blood leukocytes. As
shown in Figure 1A, the patient was
homozygous for G588, whereas each parent was heterozygous. These
results are consistent with an autosomal recessive transmission and
strongly suggest that this single nucleotide deletion is responsible
for the clinical syndrome exhibited in the patient. This deletion
predicts an alteration of the open-reading frame of the protein after
Ser195, introducing 34 random amino acids followed by a stop codon
(Figure 1B) that likely renders the protein nonfunctional.
To further assess the function of the mutant gene, we transfected skin
fibroblasts derived from the patient with either the wild-type or the
mutant (
In vitro and in vivo response to fucose therapy It has been reported that when fibroblasts, endothelial cells, and lymphoblastoid cell lines derived from LADII patients are grown in the presence of fucose, carbohydrate structures containing fucose can be induced on the cell surface.17,18 To evaluate the effect of fucose exposure on cells derived from our patient, we analyzed AAL binding to a B-lymphoblastoid cell line by flow cytometry. As shown in Figure 3, the control lymphoblastoid cell line (B7) bound AAL (left panel; Untr), and binding was further increased by exposure to 10 mM L-fucose in the medium for 5 days (left panel; Fuc). In contrast, the LADII lymphoblastoid cell line (DF1) displayed no significant binding at baseline (right panel; Untr), but, strikingly, the addition of L-fucose restored surface fucosylation to levels comparable to those found on control cells. A dose-response curve revealed that concentrations as low as 0.5 mM of L-fucose were sufficient to restore AAL binding (data not shown). These results are consistent with previous studies in cells derived from either Turkish or Arab patients,17,18 and they suggest that exposure to exogenous fucose can also restore fucosylation on LADII cells derived from this patient.
Because fucose therapy has previously been shown to be clinically
effective in one patient with LADII,18 we initiated a treatment with fucose supplements. Oral administration of L-fucose was
begun at a daily dose of 165 mg/kg divided 5 times per day and was
increased progressively thereafter (Figure
4). Within 2 weeks of the initiation of
fucose treatment, neutrophil counts decreased to the normal range. To
determine whether the clinical response correlated with improved
selectin function, we assessed the expression of the HECA-452 epitope
(which correlates with expression of sLeX) and the ability
of neutrophils to bind P- and E-selectins in a fluid-phase assay. No
sLeX or selectin binding was detected by
fluorescence-activated cell sorter (FACS) before the initiation of
fucose therapy (Figure 5; day 0).
However, as early as 8 days after the initiation of fucose treatment, a
significant increase in sLeX and P-selectin ligand
expression was detected on the patient's neutrophils. Remarkably,
E-selectin ligand expression could not be detected even after more than
230 days of treatment with fucose doses up to 1000 mg/kg per day
(Figure 5). Although P-selectin binding progressively increased to
reach levels close to those of healthy donor neutrophils (81% of the
binding of control cells on day 62), sLeX expression
increased more slowly and was still 20-fold lower by day 84 (Figure 5).
These observations are in line with those obtained from the other LADII
patient who responded to oral fucose,18 in which
E-selectin ligands were detected much later than P-selectin ligands
after fucose treatment, and they suggest a preferential incorporation
of fucose in P-selectin glycoprotein ligands over E-selectin ligands.
Fucose therapy partially restores the ability of LADII neutrophils to roll in vivo The marked improvement in neutrophil counts appeared to contrast with the selectin-binding assays, which only showed a partial rescue in selectin binding. To evaluate the ability of LADII leukocytes to roll in vivo, we isolated neutrophils from the LADII patient before and after fucose treatment. Healthy neutrophils were purified in parallel from healthy controls. Purified neutrophils were fluorescently labeled and injected through the carotid artery of immunodeficient NOD/SCID mice. Neutrophil behavior was then assessed in cremasteric venules. Under these conditions, rolling is almost entirely mediated by endothelial P-selectin.26 As shown in Figure 6A, the interacting flux of LADII neutrophils, before and 8 days after fucose treatment, was low (2.3% ± 2.3% and 1.3% ± 1.3%, respectively) compared with the average observed with neutrophils from control donors (23.8% ± 5.6%). Strikingly, on day 16 after treatment, the percentage of interacting LADII neutrophils (29.8% ± 11%) was similar to that of controls. However, detailed analysis of videotapes demonstrated a clear difference in the quality of these interactions in that fucose-treated LADII neutrophils interacted briefly and for short distances compared with the longer distances and times achieved by healthy neutrophils, as depicted in the scattergram (Figure 6B). Thus these data suggest that though the behavior of fucose-treated neutrophils is clearly abnormal in vivo on day 16, a partial recovery of P-selectin ligands alone appears to be sufficient to restore leukocyte trafficking in LADII.
Fucose therapy induces autoantibodies against neutrophils and erythrocytes After 35 days of fucose therapy, peripheral neutrophil counts decreased to levels below the adjusted normal counts (Figure 4, asterisk). We suspected that the overcorrection in the neutrophil counts might have resulted from a decreased leukocyte half-life, perhaps because of the generation of autoantibodies directed toward neoantigens expressed on the neutrophil surface. The dose of oral fucose was decreased from 975 mg/kg to 570 mg/kg per day, and the patient's serum was evaluated for the presence of antineutrophil antibodies. Samples of control and patient sera were incubated with purified neutrophils from healthy donors. Bound antibodies were detected using a Cy5-conjugated antihuman secondary antibody. As shown in Figure 7, serum from the fucose-treated LADII patient on day 41 strongly stained neutrophils by flow cytometry. Cytospin preparations revealed clustered-appearing membrane staining (Figure 7, lower inset) that was specific because no such staining was observed when neutrophils were incubated with control serum (Figure 7, upper inset). An independent reference laboratory (Neutrophil Serology Laboratory) confirmed these results and also demonstrated positive granulocyte agglutination assays (titer, 1:32) at the nadir of neutropenia (data not shown). Monoclonal antibody-specific immobilization of neutrophil antigens (MAIGA) revealed that the autoantibody was not directed against the known neutrophil autoantigens NA1, NA2, NB1, and MART (not shown). Western blot analyses of neutrophil lysates in our laboratory have failed to reveal further information about the nature of the antigen.
The possible induction by fucose therapy of fucosylated antigens on the
surfaces of erythrocytes was also a major clinical concern. This could
lead to hemolysis because LADII patients have natural antibodies
against the H antigen (Bombay phenotype). Thus, we closely monitored
hemoglobin, reticulocyte, and haptoglobin levels and the expression of
fucosylated structures on the surfaces of the patient's erythrocytes
using lectin staining. As shown in Figure
8, no detectable AAL staining was
observed on day 16 erythrocytes. However, starting from day 36 of
fucose treatment up to the writing of this report (day 260),
erythrocytes stained positively with AAL. In addition, erythrocytes
collected on day 189 reacted with 2 of 3 polyclonal anti-H sources.
Results of direct antiglobulin (Coombs) tests were always negative, and
the patient never presented clinical evidence of autohemolysis. Taken together, these results, in contrast to those of a previous
report,18 demonstrate that fucose therapy in LADII may
induce the expression of neoantigens that represent a risk for
autoimmune phenomena. Because of clinical concerns, fucose therapy has
been dose adjusted to ensure an absolute neutrophil count of 1500 or
more per microliter (Figure 4).
Psychomotor development is not improved by fucose therapy In a manner similar to that for selectin ligands on leukocytes, psychomotor development was reported to improve in the patient with the Arg147Cys mutation18,21 but not in patients with Thr308Arg.19,22 We have not yet found evidence of psychomotor improvement in our patient who, currently 15 months of age, has only recently started to crawl and babble. In addition, our patient requires nasogastric tube feeding because of poor oropharyngeal coordination. Given that only 25% of the serum fucose concentrations is found in the cerebrospinal fluid,18 it is possible that psychomotor improvement in our patient is hampered by the limited doses of administered fucose, owing to the aforementioned complications.
The 5 previously reported cases of LADII were of Middle Eastern
descent.16 Four Arab patients from Israel and one Turkish patient from Germany shared similar characteristic clinical features, including severe mental retardation, profound leukocytosis with recurrent infectious episodes, defective selectin ligand formation with
normal Major advances have recently been made in the therapy and understanding of this disease. The first came from the observation that exogenous fucose could overcome the fucosylation defect in culture17,27 and subsequently in a patient.18 Treatment of the Turkish LADII subject with high doses of oral fucose produced a rapid lowering in the peripheral neutrophil counts, which coincided with the induction of selectin ligand expression on leukocytes but, remarkably, did not induce the expression of the H antigen on erythrocytes. In addition, improved psychomotor development was seen as a result of fucose therapy. The fact that none of the Arab patients responded to fucose treatment19,20 suggested that LADII in the Arab kindred had a different molecular basis. The recent cloning of a putative GDP-fucose transporter, whose predicted structure encompasses 10 transmembrane domains, brought a molecular explanation for this differential response because Arab and Turkish patients exhibited distinct mutations at the GDP-fucose transporter locus. The Turkish subject had a point mutation (Cys439Thr) causing the replacement of arginine 147 by a cysteine (Arg147Cys) in the fourth transmembrane domain of the transporter, whereas the GDP-fucose transporter gene from 3 Arab patients contained a Cys923Gly mutation leading to a missense change from threonine to arginine (Thr308Arg) in the ninth transmembrane domain.21,22,25 It was thought that the Arg147Cys mutation might lead to a reduced affinity of the transporter for GDP-fucose that could be compensated by elevating cytosolic GDP-fucose levels, thus explaining the clinical response in the Turkish patient.29 This hypothesis was supported by kinetic studies of GDP-fucose import into Golgi preparations in which both Arab- and Turkish-derived cell extracts showed a reduced maximal velocity (Vm) of the saturable transport component, but only Golgi vesicles from the Turkish patient displayed a nonsaturable component.20,27 Given that the patient described in this report came from a different
ethnic background, we suspected that we might find a novel mutation.
Indeed, sequencing of cDNA and genomic DNA from our patient and his
parents revealed a single base deletion ( The results of the selectin ligand assays suggested that only a partial restoration of P-selectin ligand activity can fully restore leukocyte homeostasis in LADII. We have correlated these in vitro assays with the behavior of fucose-treated LADII neutrophils in vivo using intravital microscopy. Our results show that despite a rapid and complete normalization of peripheral neutrophil counts, individual neutrophils still displayed marked defects in their ability to interact with P-selectin in cremasteric venules. These results also underscore the limitations in the sensitivity of fluid-phase binding assays because little difference was found in vitro between days 8 and 16 of fucose treatment (Figure 5), whereas significant improvement in the neutrophil interactions with the vessel wall (and sustained clinical response) were observed in vivo after day 8. It is interesting that in contrast to P-selectin ligands, E-selectin
ligands were never induced in our patient. In the report by Marquardt
et al,18 E-selectin ligand expression required approximately a 2.5-fold higher dose of L-fucose (1665 mg/kg per day)
than that needed to induce P-selectin ligands. These results suggest a
preferential fucosylation of P-selectin ligands in neutrophils and that
a higher Golgi concentration of fucose may be required for the
fucosylation of E-selectin ligands. Preferential fucosylation has been
described at the fucosyltransferase level. For example, the 2 known
leukocyte fucosyltransferases (FucTIV and FucTVII) exhibit a
differential preference for distal Importantly, we found that the induction of fucosylation in our patient produced 2 potentially serious complications. The first was the appearance of autoimmune neutropenia that likely originated from the induction of neoantigens on the surfaces of neutrophils. The neutropenia responded to a reduction of the fucose intake (Figure 4), which lends support to a cause-and-effect relationship between these 2 phenomena. The second complication was the documented expression of fucosylated glycans on the surfaces of erythrocytes. Because the patient has a Bombay phenotype (absence of H antigen and presence of anti-H antibodies), the expression of the H antigen could potentially produce severe autoimmune hemolysis. Although we observed that fucose therapy also induced the expression of fucosylated structures (as detected by AAL) including the H antigen (as detected by specific antisera), no evidence of hemolysis was observed (as assessed by reticulocyte counts or haptoglobin and hemoglobin levels), and the patient never required any transfusion. These potentially severe complications highlight the importance of close monitoring during fucose therapy. Future structure-function analyses of the GDP-fucose transporter will be useful to understand the mechanisms behind the variable response to fucose therapy.
We thank Drs Anjali Kumar and John Lowe for providing reagents, Dr Marion E. Reid at the New York Blood Center for confirming the Bombay typing and evaluation of red cell antigens, and Dr Yande Kuang for providing the B7 lymphoblastoid cell line. We also thank Dr Luis Martinez and Goutham Narla for help with molecular biology and Drs Steven Simonte and Yoshio Katayama for help in obtaining blood samples from the patient and healthy donors, respectively.
Submitted September 18, 2002; accepted October 10, 2002.
Prepublished online as Blood First Edition Paper, October 24, 2002; DOI 10.1182/blood-2002-09-2840.
Supported by National Institutes of Health grants FDA1697, AI-48693, and AI-46732 (C.C.R.) and DK-56638 and HL-69438 (P.S.F.).
The publication costs of this article were defrayed in part by page charge payment. Therefore, and solely to indicate this fact, this article is hereby marked "advertisement" in accordance with 18 U.S.C. section 1734.
Reprints: Paul S. Frenette, Department of Medicine, Mount Sinai School of Medicine, Box 1079, One Gustave L. Levy Place, New York, NY 10029; e-mail: paul.frenette{at}mssm.edu.
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In vivo neutrophil and lymphocyte function studies in a patient with leukocyte adhesion deficiency type II.
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1994;84:1635-1639 14. Phillips ML, Schwartz BR, Etzioni A, et al. Neutrophil adhesion in leukocyte adhesion deficiency syndrome type 2. J Clin Invest. 1995;96:2898-2906[Medline] [Order article via Infotrieve]. 15. Becker DJ, Lowe JB. Leukocyte adhesion deficiency type II. Biochim Biophys Acta. 1999;1455:193-204[Medline] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Abstract
Introduction
2 integrins is
defective,
) or
LADII (
) neutrophils from day 16 reveals transient interactions of
LADII neutrophils compared to those from a healthy donor.
