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1 functional diversity is lost after neonatal thymectomy.
2 ow chimeras prepared after complete surgical thymectomy.
3 s by combined cyclophosphamide treatment and thymectomy.
4 imilar to the previously described effect of thymectomy.
5 n, and these cells disappear following early thymectomy.
6 hymus prevents the induction of disease post-thymectomy.
7 utes of Health-funded international trial of thymectomy.
8 ult male C57BL/6 mice with and without prior thymectomy.
9 cells, and rapidly decreased after complete thymectomy.
10 reduction surgery, lung transplantation and thymectomy.
11 n target peripheral T cells up to 2 mo after thymectomy.
12 eated with FK506, anti-CD4 mAbs (GK1.5), and thymectomy.
13 atients before and from 27 to 517 days after thymectomy.
14 for MG decreased thymopoiesis independent of thymectomy.
15 nt ways: total body irradiation and neonatal thymectomy.
16 fficacy is questionable or unproved, such as thymectomy.
17 loantigenic stimulation 2 wk after the adult thymectomy.
18 ejected and survival was not affected by the thymectomy.
19 frequency that is enhanced significantly by thymectomy.
20 d MG patients studied at varying times after thymectomy (1 day to 41 years), we found no significant
23 2 days of CyA underwent either (1) a partial thymectomy 21 days before kidney transplantation (day -2
24 urse of cyclosporine (CyA), and that a total thymectomy 21 days before transplantation abrogates the
26 treated with modified regimens that omitted thymectomy, 3 Gy TBI, anti-Thy1.2, and anti-NK1.1 mAbs,
27 prognosis was good, with a reduced need for thymectomy (6.3% vs 19.2%) and a high proportion of pati
30 IL-7R, or devoid of T cell renewal via adult thymectomy, all exhibited significant increases in TCE i
31 ally transplanted into recipients undergoing thymectomy alone or recipients undergoing thymectomy plu
32 st, using the complementary methods of early thymectomy and adoptive transfers, we found that PTEN-de
34 c age of residual PTK7 (+) T cells following thymectomy and may also explain in part the prematurely
37 etes, induced in rats by a protocol of adult thymectomy and split-dose gamma irradiation, can be prev
38 with naive CD4+CD25- effector T cells after thymectomy and T-cell depletion in CBA mice that receive
39 rgan-specific autoimmune disease after day 3 thymectomy and the effector function of cloned autoantig
40 responses could first be detected 5 wk post-thymectomy and were accompanied by high background respo
41 ed through a partial (n=6) or complete (n=2) thymectomy, and growth of the autologous thymic graft wa
42 the response to extended cervicomediastinal thymectomy as a component of the integrated management o
47 primary response to H-Y for some time after thymectomy but lost this ability at approximately 6 mo.
48 press not only the induction of disease post-thymectomy, but can also efficiently suppress disease in
49 ast, mice that were primed to H-Y just after thymectomy continued to display immunological memory to
54 ting to the relevance of the thymic effects, thymectomy decreases by approximately 50% the bone loss
57 the T cell pool in fetal life, but postnatal thymectomy does not lead to immunodeficiency in humans.
61 s' most recent 100 consecutive transcervical thymectomies for nonthymoma-associated MG was performed
62 ecutive patients who underwent trans-sternal thymectomy for symptomatic myasthenia gravis from 1969 t
64 ne (6.15 vs. 8.99, P<0.001); patients in the thymectomy group also had a lower average requirement fo
65 between groups (P=0.73), but patients in the thymectomy group had fewer treatment-associated symptoms
77 ll with acute hepatitis B after undergoing a thymectomy in which a thoracic-surgery resident who had
78 lls in PG and SMG following short-term adult thymectomy indicated that immature salivary gland T cell
79 ls that inhibit SAT were eliminated by day 3 thymectomy, indicating they belong to the subset of natu
80 A/J and (C57BL/6J x A/J)F1 hybrids, neonatal thymectomy-induced autoimmune ovarian dysgenesis (AOD) i
81 uggests that, as in adult myasthenia gravis, thymectomy is a viable therapeutic option for selected c
83 and naive CD4 T cells, is enhanced by 3-day thymectomy, is independent of IL-7, and requires a class
85 ment, compared to conventional trans-sternal thymectomy, neither the pathologic diagnosis (presence o
90 of donor-specific thymus combined with adult thymectomy of recipients enhances the tolerogenic effect
92 plant tolerance, which was then abrogated by thymectomy of the recipient before intravenous injection
95 ay 0 host-type thymocyte infusions following thymectomy on day -21, developed donor-specific hyporesp
96 ithout changes in thymic volume), (3) a sham thymectomy on day -21, or serial sham thymic surgery on
97 Female (C57BL/6xA/J)F(1) mice undergoing thymectomy on day 3 after birth (d3tx) developed autoimm
99 have studied patients with MG for effects of thymectomy on peripheral blood (PB) naive (CD45RA(+), CD
100 le tolerance induction, because either prior thymectomy or a series of thymic biopsies induce a spont
101 Suppression of resistance of recipients by thymectomy or injections of granulocyte colony-stimulati
102 ssential for tolerance because pretransplant thymectomy or peritransplant depletion of CD25(+) cells
104 nosuppressive-conditioning regimen including thymectomy or thymic irradiation, extracorporeal immunoa
105 equently performed surgical procedure (e.g., thymectomy) or in cases where there was no predominant p
106 myasthenic patients, for whom treatment with thymectomy, plasmapheresis, and conventional immunothera
108 ng thymectomy alone or recipients undergoing thymectomy plus either CD4+ or CD8+ T cell depletion.
110 ic rats before the onset of disease by adult thymectomy plus short-term anti-CD8alpha mAb treatment.
111 r-old man with myasthenia gravis and a prior thymectomy presenting with 2 months of diffuse, involunt
115 sponse of patients with myasthenia gravis to thymectomy primarily with respect to the bivariate endpo
117 ntinuous isotype-matched control mAb, 3) the thymectomy/pulse anti-CD8alpha regimen, or 4) no treatme
118 and contrast-enhanced CT groups had similar thymectomy rates (P = .97) and disease-related symptom t
119 ted with RIB 5/2 plus an i.v. alloantigen +/-thymectomy received kidney transplants after 40 days.
124 ons most when thymopoiesis was active before thymectomy (six of six patients), but had little effect
125 aboons underwent a conditioning regimen with thymectomy, splenectomy, and anti-monkey CD3 antibody co
126 ppressive conditioning regimen that included thymectomy, splenectomy, extracorporeal immunoadsorption
127 patient with myasthenia gravis treated with thymectomy subsequently developed extensive granulomatou
128 days, whereas anti-CD4, in combination with thymectomy, synergistically prolonged survival of pancre
130 onships between performance on the UPSIT and thymectomy, time since diagnosis, type of treatment regi
134 c graft-vs-host reaction (synGVHR) and timed thymectomy (Tx) assays revealed that autoeffector T cell
135 s were created by subjecting juvenile RMs to thymectomy versus sham surgery, respectively, followed b
136 ereas the use of extended cervicomediastinal thymectomy was associated with a greater than twofold ch
140 ldren and adolescents who underwent neonatal thymectomy, we demonstrate that the naive CD4+ T cell co
141 s without adoptive transfer, irradiation, or thymectomy, we developed genetically modified mice that
144 at their numbers progressively decline after thymectomy with a half-life of approximately 2 weeks.
145 th a history of thymoma or thymic neoplasms, thymectomy within 12 months before screening, or use of
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